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Directions for use, Welch Allyn Connex® Vital Signs Monitor 6000

1. S2 6000 2 Literature Documentation Part Number 103730 4600 90E 6000 150E Directions for Use 03501 03604 03605 03606 03607 03608 03609 03650 03651 03652 Welch Allyn Connex Vital Signs Monitor 6000 Series Description Patch cable 100 Patch cable 5 Box set packaging empty USB memory stick Description Comprehensive partnership program 1 year Comprehensive partnership program 2 years Biomed partnership program 1 year Biomed partnership program 2 years Description CD Directions for Use Service Manual Multi lingual Blood Pressure Accuracy and Variability Card English In service CD Directions for Use Printed Copy English Directions for Use Printed Copy French Directions for Use Printed Copy German Directions for Use Printed Copy Dutch Directions for Use Printed Copy Portuguese Directions for Use Printed Copy Spanish Directions for Use Printed Copy Simplified Chinese Directions for Use Printed Copy Swedish Directions for Use Printed Copy Italian Directions for Use Printed Copy Danish Directions for use Appendix 145 Part Number Description 103653 Directions for Use Printed Copy Polish 103654 Directions for Use Printed Copy Finnish 103655 Directions for Use Printed Copy Greek 03656 Directions for Use Printed Copy Norwegian 104187 Directions for Use Printed Copy Traditional Chine
2. 20 0 26 25 0 34 32 0 43 40 0 55 Circumference cm 3 3 5 6 Circumference in 3 5 5 1 4 7 6 3 59 83 79 102 9 8 13 4 12 6 16 9 157 217 Circumference in 13 22 66 Patient monitorin g Cuff Size Circumference cm Circumference in E02 EO 3 EO 4 EQ 5 M ulti pack Welch Allyn Connex Vital Signs Monitor 6000 Series 4 2 7 1 1 6 2 8 5 4 9 1 2 1 3 6 6 9 11 7 24 46 8 9 15 0 3 5 5 9 1 of each 1 of each For ordering information see Approved Accessories in the Appendix Position the cuff Note N A A A The monitor and cuffs were validated using the bare upper arm site WARNING Patient injury risk Do not use the NIBP for continuous monitoring without frequently checking the patient s limb When a patient is being monitored frequently or for a prolonged period regularly remove the cuff to inspect it and to check the cuff site for ischemia purpura or neuropathy WARNING Inaccurate measurement risk Do not place the cuff where it can disturb proper circulation Do not place the cuff on any area where circulation is compromised or on any extremity used for intravenous infusions Do not use an SpO2 finger clip sensor and a blood pressure cuff simultaneously on the same limb Doing so may cause a temporary loss of pulsatile flow resulting in either no reading or an inaccurate SpO2 or pulse rate until the flow re
3. 110 Standards and compliance Welch Allyn Connex Vital Signs Monitor 6000 Series Electrical Equipment WEEE If this product is contaminated this directive does not apply For more specific disposal or compliance information see www welchallyn com weee or contact Welch Allyn Customer Service at 44 207 365 6780 General radio compliance The wireless features of this monitor must be used in strict accordance with the manufacturer s instructions as described in the user documentation that comes with the product This device complies with Part 15 of the FCC rules and with the rules of the Canadian ICES 003 as described below Federal Communications Commission FCC This device complies with part 15 of the FCC Rules Operation is subject to the following two conditions e This device may not cause harmful interference e This device must accept any interference received including interference that may cause undesired operation This equipment has been tested and found to comply with the limits for a Class B digital device pursuant to Part 15 of FCC Rules These limits are designed to provide reasonable protection against harmful interference in a residential installation This equipment generates uses and can radiate radio frequency energy If not installed and used in accordance with the instructions it may cause harmful interference to radio communications However there is no guarantee that interference will not occur
4. 3 digits Motion z 5 digits 7096 to 10096 Adults Pediatrics No motion 2 2 digits Neonates No motion 3 digits Adults Pediatrics Neonates Motion 3 digits Low Perfusion 0 02 to 20 2 digits SpO2 measurement accuracy can only be evaluated in vivo by comparing pulse oximeter readings with Sa02 measurements obtained from simultaneously sampled arterial blood made using a laboratory CO oximeter SpO2 accuracy was validated through breathe down equivalent testing by Covidien using electronic measurements to prove equivalence to the Nellcor N600x predicate device The Nellcor N600x predicate device was validated by performing human subject breathe down clinical trials 0 03 to 20 20 to 250 beats per minute bpm 3 digits 70 to 100 Adult Pediatrics 2 digits Neonate 3 digits Low Perfusion 0 02 to 20 2 digits Directions for use Specifications 105 Sp02 specifications refer to sensor manufacturer s directions for use for additional information Functional tester A WARNING Functional testers cannot be used to assess the accuracy of a pulse oximeter monitor 1 Some models of commercially available bench top functional testers and patient simulators can be used to verify the proper functionality of Nellcor pulse oximeter sensors cables and monitors See the individual testing device s operator s manual for the procedures specific to the model of tester being used Whi
5. Make sure that the monitor is powered on Remove the ear thermometer from the accessory dock Locate the probe cover box in the accessory dock R Firmly push the probe tip into the probe cover box When the probe cover is in place the thermometer turns on automatically 9 Wait for the ready beep and three dashes to appear on the thermometer display Fit the probe snugly into the ear canal and then push and release the Start button e fthe probe is positioned correctly in the ear canal the ExacTemp light flashes When the thermometer detects an accurate measurement the ExacTemp light is continuously on a long beep signals the end of the measurement and the display shows the result e fthe probe is positioned incorrectly in the ear canal or is moved during the measuring process the ExacTemp light goes out a sequence of short beeps sounds and the error message POS position error appears 7 When you are finished taking the temperature press the ejector button to eject the used probe cover 8 Return the thermometer to the accessory dock The LED on the dock flashes while the measurement is being transferred After the transfer is complete the temperature and the temperature scale appear on the Home tab according to the monitor settings Note Only the latest measurement is transferred to the monitor Note Measurements that have already been transferred to the monitor cannot be transferred again For more infor
6. Note For monitors configured with SpHb the cable used to monitor SpHb uses the same port and also measures SpO2 Disconnect the SpO2 cable 1 Place your thumb and forefinger on the cable connector Note Always grasp the cable by the connector Do not pull on the cable itself 2 Squeeze the side tabs until the connector releases 3 Pull the connector away from the connector port Attach an accessory A CAUTION Accessories attached to this monitor must run on battery power Do not use any accessory s external power supply when it is attached to the monitor 1 On the rear of the monitor loosen the screw on the USB door and open it 2 Attach the accessory s USB cable into an unused USB port on the monitor The example below shows how to attach cables for a barcode scanner and a mobile stand light For information about attaching any other accessory refer to the instructions provided with the accessory A CAUTION Connect cables in a manner that minimizes entangling we 3 Close the door and tighten the screw Note Some accessories require a license to enable them for use These accessories are packaged with an authorization code and instructions for activating the license using the Welch Allyn Service Tool For more information refer to the instructions and the service tool installation guide Directions for use Setup 25 Detach an accessory 1 On the rear of the monitor loosen the screw on the USB door and
7. 56 Alarms Welch Allyn Connex Vital Signs Monitor 6000 Series Reset pause or turn off audio alarms Audio alarm characteristics After you reset an audio alarm some tones do not return but others return after a pause interval if the condition that caused the alarm persists Settings in the Advanced tab determine the length of the pause interval If anew alarm condition occurs during a pause interval a new audio tone occurs If an audio alarm is not paused or turned off after a period of time a buzzer accompanies the tone Pause or turn off an audio alarm 1 In the Device Status area touch A o Visual indications remain in the parameter frame until the condition is corrected or until the next measurement is taken ES In the Device Status area if the icon changes to i and the message remains the timer counts down and the audio tone returns after a pause A interval You can touch e again to restart the timer If you responded to an NIBP alarm and multiple NIBP limits have been exceeded the first audio tone and message go away but another NIBP limit message shows with a countdown timer A new NIBP audio tone sounds after A the countdown unless you touch e to dismiss each remaining NIBP limit message If multiple alarms are active a multiple alarm toggle will appear in the Device Status area Respond to multiple alarms as follows gt Touch Read the alarm message for the second alarm in t
8. Accesses the patient list patient summary patient modifiers and manual parameters e Alarms Accesses global alarm response and settings controls plus alarm limits settings available only in Monitor mode e Review Prints deletes and sends patient data e Settings Accesses device configuration settings To navigate to a tab touch the tab in the Navigation area with the corresponding name The active tab is highlighted Display lock The display lock prevents clinician input which may be useful when cleaning the display Note The lock feature is not a security mechanism The display locks when any of the following occur e You touch Lock display now e No interaction with the monitor occurs for the period specified in the Display tab Use the Advanced tab to set or change the time it takes for the display to lock This requires the Advanced settings access code Lock the display Follow these steps to touch the screen without activating the controls 1 Touch the Settings tab 2 Touch the Device tab 3 Touch Lock display now The following occurs e The Home screen appears Directions for use Navigation 35 i Patricia J Jones O 03 00 12 29 2013 Continuous all EEE MIEDO 1 10 IPI 0 10 a 4 A 90 isel TEMPERATURE A 101 57 38 6 C PATIENT HEIGHT WEIGHT PAIN 13579 WelchAllyn Connex amp e Atitle bar with a lock icon amp replaces the Navigation area at the bottom of the
9. The monitor retrieves the patient list from the network 3 From the patient list touch the patient s identifier name ID number or location The patient s identifier is determined in Advanced settings 4 Touch Select Note In the Spot Check and Triage profiles previous patient data will be overwritten by a new save In the Monitor profile selecting a new patient will clear the current patient data and readings Patient data can be sorted in ascending or descending order by selecting the heading row and touching A or V Manage patient records Patient records can be sent to the network printed or deleted 1 Touch the Review tab Note Measurements that triggered a physiological alarm are highlighted on this tab Patient Yate Time NIBP Temp PR SpO2 SpHb Ht Wt P RR NN amp 12 31 2011 13 41 120 68 85 36 2 0 96 13 9 182 9 89 4 3 15 uu Lu Review HELL 2 Select patients by touching the check box next to their names Directions for use Patient data management 49 3 Touch Send to transmit the records to the network Print to print the records or Delete to permanently remove the records as desired A A Note Note Note Note Print patient data CAUTION Verify patient identity on the monitor after manual or barcode entry and before printing or transferring patient records CAUTION Always visually verify the printed patient records The EX icon indicates the records ha
10. To enter the clinician name touch located at the right of the text field and enter characters You can enter up to 32 characters for the clinician s first and last name Enter only 1 character for the middle initial To enter the clinician ID use one of these methods e Touch mm and enter the ID e Scan the clinician s barcode with a barcode scanner The scanned ID appears in the field If prompted enter your system password in the Authentication pane Touch OK to save your entries and return to the Home tab ault configuration Touch the Settings tab Touch the Device tab Enter or adjust the desired settings you want to add or change Note The new settings appear as they are completed but are temporary until they are saved Touch Save as default Touch OK to confirm that you want to overwrite your previous settings and replace them with your current settings in the startup default configuration Or touch Cancel to retain the previous settings The new settings are stored as the default startup settings once you restart the monitor Note If your monitor is connected to the network the date and time settings are synchronized with the network settings Note The date and time stamps on saved patient measurements will adjust in response to new date and time settings 31 Navigation The monitor screen provides the interface that you use to complete your workflow You access the monitor s features by to
11. accessories The monitor and the accessories are not heat resistant WARNING Liquids can damage electronics inside the monitor Prevent liguids from spilling on the monitor If liguids are spilled on the monitor Power down the monitor Disconnect the power plug Remove battery pack from the monitor Dry off excess liquid from the monitor SIS ca Note If liguids possibly entered the monitor remove the monitor from use until it has been properly dried inspected and tested by qualified service personnel 5 Reinstall battery pack 6 Power on the monitor and verify monitor functions normally before using it If liquids enter the printer housing 1 Power down the monitor 2 Disconnect the power plug 3 Remove battery pack from the monitor 4 Remove and discard the paper roll 5 Clean and dry the inside of the printer housing Note The printer housing has a drain tube that directs liquids down and out the bottom of the device If liquids possibly entered other openings in the monitor remove the monitor from service until it has been properly dried inspected and tested by qualified service personnel 6 Install a new roll of paper 7 Power on the monitor and verify that the monitor functions normally before using it Clean on a routine basis according to your facility s protocols and standards or local regulations If the monitor is on lock the display and disconnect the AC power cord The following agents
12. arrow keys or the keypad 5 Touch the Home tab Directions for use Patient monitoring 93 The new alarm settings display in the Alarm Limit control button Manual parameters frame The Manual parameters frame located in the lower right of the Home tab supports manual entry of parameters and displays measurements taken by some accessories Note Manual parameters are not available in the Triage profile Note Body mass index BMI is only available with an attached weight scale that calculates BMI Note When a measurement is transferred from an attached weight scale to the monitor the measurement displayed on the monitor is within one decimal place 0 1 of the measurement displayed by the weight scale Note You cannot manually enter temperature on a monitor configured with a SureTemp Plus temperature module Enter manual parameters Note The Manual parameters frame enables you to enter measurements taken manually and displays measurements taken by some accessories You can select and configure the parameters in Advanced settings Only four parameters appear in the Manual parameters frame A CAUTION Weight scales attached to this monitor must be running on battery power battery type is specified in the weight scale manufacturer s directions for use Do not use the weight scale s external power supply 1 From the Home tab touch anywhere within the Manual parameters frame EIGHT WEIGHT PAIN List Summary Modifiers M
13. following Advanced settings or tube use to match patient NIBP measurement is not 1 Patient type is Pediatric or Adult type available 2 Tube type is 2 3 Algorithm is SureBP Sp02 and SpHb messages Message Possible cause Suggested action Sp02 not functional Call for A module error has occurred Try a new cable sensor pair Service Call for service Searching for pulse signal High The SpO2 sensor is not attached to the patient s Touch the alarm icon or the SpO2 priority alarm finger frame to dismiss the alarm Set SpO2 alarm limits to OFF Reattach the SpO2 sensor to the patient s finger Attach SpO2 sensor to monitor The sensor was not detected Check the sensor connection Replace the SpO2 sensor Replace the SpO2 sensor The SpO2 sensor is faulty or expired Replace the SpO2 sensor Directions for use Message Replace the SpO2 cable Low Sp02 signal quality Check sensor Low SpHb signal quality Check sensor Low perfusion Check sensor Possible cause No SpO2 sensor is connected The cable is faulty or expired The cable is faulty or expired Poor sensor placement on the patient Poor sensor placement on the patient Poor sensor placement on the patient Troubleshooting 133 Suggested action Connect an SpO2 sensor Replace the cable Replace the cable Remove the sensor from the patient and reapply Remove the sensor from the patient and reapply Remove the sensor from
14. 12 31 2011 amp 07 46 Pain 0 102 68 6 78 97 RR 12 bpm 12 31 2011 amp 07 46 105 67 79 80 96 12 31 2011 amp 07 46 100 64 76 77 97 Continuous monitoring report Spot Check report Delete a patient from the list Touch the Patients tab 2 From the List tab touch the patient record you want to delete Touch Delete At the Delete Confirmation window touch OK to permanently delete the selected patient Touch Cancel to cancel the deletion Note Deleting a patient from the Patients List does not delete saved records Touch Review to see or delete saved records Note For monitors connected to the network deleting a patient on the monitor does not affect data on the network Modifiers The Modifiers tab enables you to enter additional information for current measurements List Summary Modifiers Manual NIBP 02 Cuff site Flow rate Cuff size Concentration Patient position Method Set modifiers 1 Touch the Patients tab Directions for use Patient data management 51 2 Touch the Modifiers tab Adjust the NIBP O2 and Temperature settings as required 4 Touch OK to accept the changes and return to the home screen or touch Clear to delete all entries The Modifier settings clear after a power cycle after you clear the Home tab or after you select a new patient 52 Patient data management Welch Allyn Connex Vital Signs Monitor 6000 Series 53 Alarms The monit
15. 13 seconds The temperature frame continues to display the temperature in degrees Fahrenheit and degrees Celsius even after the probe is returned to the probe well TEMPERATURE 97 9 F 36 69C Note To switch to the Direct mode touch E after the Predictive mode measurement is acquired The temperature frame in the lower left corner changes to MODE Direct as it switches to the Direct mode The monitor sounds a tone to indicate the start of a Direct measurement Once you are in the Direct mode continue to separate the buttocks and hold the probe in place throughout the measurement process Note The monitor does not retain Direct mode temperatures in memory Therefore it is important to note the temperature before removing the probe from the measurement site and then manually record it in the patient record Remove the probe after the temperature measurement is complete and firmly press the eject button on the top of the probe to release the probe cover Return the probe to the probe well Wash your hands to reduce the risk of cross contamination 82 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series Braun ThermoScan PRO 4000 thermometer and accessory dock The thermometer and accessory dock enable you to transfer an ear temperature measurement to the monitor The dock also charges the thermometer battery Read the thermometer manufacturer s directions for use before attempting to co
16. Keyboard c ecc eec ote iet dtr t ettet NIE 42 Keyboard O 42 Enter a letter or number sese eret been rut ere dete esi 44 Enter a symbol or special character 0cccee cee ceeeececceeceeceeeceeeeeeeeeeeeeeeeeeeneees 44 Entera diaeritical mark arreen re ette tI eo te IR CED E ARES 44 Closethe XKeyboard tette Y YY Patio eter E 45 Use a bareode scanlher e e eed b e petat ie edet ets 45 Patient data management cooonnccccncccconononenenonennnnnnnnnnnnnnnnnnnnnnnnnnannnznnnnnns 47 Add a patient to the patient list ssssssssss mee 47 Load patient data with the barcode scanner sssssssssssse 47 Selecta Dati Hos soo tt dear dct uoa rues dsl en pa TU aee OG 48 Mariage patientirecords sete e Dd cte eire bite ne een 48 Print patienti o 49 Pintera o HER EE a ee tti 49 Delete a patient from the list ssssssssssssse enne 50 MOI oit Wd YD d WEM MERC de aa d e te wires 50 Set aoditl6ks e LE 50 Ala MS TETTE D UELUT 53 Reset pause or turn off audio alarms 20 0 eee ii YIII LLALL RL ee 56 Adjust vital Sigh alar MS citar tenet ea fe E ERE UO 57 Modify audio alarm notification eera n a E eene 57 Alarm messages and priorities sssssssssssssseeeeeeme n 58 Nurse call ttt PUPPI ett 61 Patient moni el TRO PEE DT LO SE DU 63 NEP 24 d nitet a tede ite date te e ate dut 63 Temperature ze op MER MERE OE REA 72 Nue 84 loin S MATE TRE fT du PTT TERRENCE CARERE 89 P lserate Tr mmescsanen e wd a e t
17. Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears Touch the Parameters tab Touch the SpHb tab Specify settings Setting Action Description Reference Select arterial or venous as the calibrated reference source Unit of measure Select the primary unit of measure for the SpHb display on the Home tab 124 Advanced settings Welch Allyn Connex Vital Signs Monitor 6000 Series Default averaging Select the default moving window of time used by the parameter to calculate the SpHb value and update the display short approximately 1 minute medium approximately 3 minutes or long approximately 6 minutes Trend view time Select the period displayed in the SpHb trend graphic on the Home tab 5 Doone of the following To continue in the Advanced Settings touch another tab To exit the Advanced tabs and return to the Home tab touch Exit Specify advanced pulse rate settings 1 Access the Advanced Settings a b C d Touch the Settings tab Touch the Advanced tab Enter the Advanced settings code Touch OK The General tab appears 2 Touch the Parameters tab Touch the Pulse rate tab 4 Specify settings Setting Action Description Display source Select this to show the source of pulse rate measurements NIBP or SpO2 on the Home tab 5 Doone ofthe following To continue in the Advanced Settings touch another tab To exit the A
18. WARNING Cross contamination or nosocomial infection risk Clean and disinfect the monitor on a routine basis according to your facility s protocols and standards or local regulations Thorough hand washing before and after contact with patients greatly reduces the risk of cross contamination and nosocomial infection CAUTION United States Federal law restricts this monitor to sale distribution or use by or on the order of a physician or licensed healthcare professional CAUTION Electromagnetic interference risk The monitor complies with applicable domestic and international standards for electromagnetic interference These standards are intended to minimize medical equipment electromagnetic interference Although this monitor is not expected to present problems to other compliant equipment or be affected by other compliant devices interference issues still may occur As a precaution avoid using the monitor in close proximity to other equipment In the event that equipment interference is observed relocate the equipment as necessary or consult manufacturer s directions for use CAUTION Use only a Class grounded AC power supply cord for powering this monitor CAUTION Do not use a long press of ZO to power down the monitor when it is functioning normally You will lose patient data and configuration settings CAUTION Never move the monitor or mobile stand by pulling on any of the cords as this may cause the monitor to tip over or may
19. above the recommended separation distanced in meters m can be estimated using the equation applicable to the frequency of the transmitter where Pis the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer Note 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people 117 Advanced settings The Advanced tab provides password protected access to the monitor s Advanced settings or Admin mode enabling nurse administrators biomedical engineers and or service engineers to configure specific features The Advanced tab also presents read only information about the monitor Note You cannot enter the Advanced settings if sensors or physiological alarms are active or if vital sign measurements are displayed Intervals Device Clinician Profiles Advanced Advanced settings code SN Hardware version xke P2 Model Software version 1 2 3 Asset tag 4 amb 6 MAC address j Configuration Ethernet 00 1A FA FF FC 00 NIBP MAC 00 00 00 00 00 00 7 8 9 PULSE RATE SpO2 IP address o SENSN oo hene 0000 Radio 0 0 0 0 General Specify the language 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter
20. accessory cable management system Clean on a routine basis according to your facility s protocols and standards or local regulations Note Disinfect according to your facility s protocols and standards or local regulations 100 Maintenance and service Welch Allyn Connex Vital Signs Monitor 6000 Series Specifications Physical specifications 101 Protection classifications all monitor configurations Characteristic Electrical rating Duty cycle Type of protection against electric shock Degree of protection against electric shock for parts applied to patients Recovery time following defibrillator discharge Flammable anesthetics Degree of protection provided by the enclosure with respect to harmful ingress of liguids Height Width Depth Weight including battery Graphical display resolution Display area Pixels Specification 100 240 V AC 50 60 Hz 1 5 0 8 A Continuous operation Class equipment protectively earthed with double insulation Type BF defibrillator proof IEC EN 60601 1 2nd Edition Less than or egual to 10 seconds WARNING Not suitable for use with flammable anesthetics A IPXO Non protected according to EN IEC 60529 Pulse oximeter equipment complies with ISO 9919 Cl 44 6 Ingress of liquids tests and EN IEC 60601 1 60601 2 30 60601 2 49 Cl 44 3 Spillage tests 10 in 25 4 cm 11 in 29 2 cm 6 in 15 7 cm 9 5 Ib 4 3 kg 8 in H x 4
21. call for service Replace the paper If the problem persists call for service Wait for the print head to cool down and retry If the problem persists call for service Call for service A hardware failure occurred in the power supply The printer does not identify itself correctly The printer cannot communicate with the monitor No printer wrong printer An external printer is plugged into a USB port The monitor is printing the records selected on the Review tab Unplug the external printer Acknowledge the number of records printing or touch Cancel to interrupt printing 138 Troubleshooting Welch Allyn Connex Vital Signs Monitor 6000 Series Message Possible cause Suggested action Note The number of records requested appears in the message and counts down during printing Printing report please wait The printer needs more time to complete a print Wait for the print job to print job when the Automatic print on completely interval control has been enabled Problems and solutions The problems addressed in this table do not generate alarm or information messages on the monitor Problem Possible cause Suggested action No SpHb value is displayed An SpO2 only cable is connected to the monitor Replace the Sp02 only cable with an Sp02 SpHb Masimo Rainbow cable The SpHb cable has expired Replace the SpHb cable Note A technical alarm appears Poor sensor placement on the patient Remove the sensor from t
22. can scan a patient s barcode from the Home tab or the Summary tab The scanned ID appears in the Patient frame on the Home tab and in the Patient ID field on the Summary tab Before you scan a barcode on the Summary tab touch the keyboard icon in the Patient ID field To return to the Home tab and begin taking patient measurements touch OK Scanning a clinician ID while the Clinician ID pane is open places the scanned ID into the Clinician ID section of the Device Status area Touch OK to return to the Home tab and to begin taking patient measurements Use the Advanced settings Data Management tab to change the appearance of the Clinician ID if you do not want your ID to appear in the Device Status area This reguires the Advanced settings access code However this information is still retained in the monitor memory for recall printing or to send measurements electronically to the network 47 Patient data management Patient data is managed through the Patients tab From this tab you can do the following Retrieve a patient list from the network or manually create a patient list Select a patient from the list Scan a patient ID with the barcode scanner and return an Admit Discharge Transfer ADT patient name match Enter additional patient information such as modifiers and manual parameters A CAUTION Verify patient identity on the monitor after manual or barcode entry and before printing or transferring patient recor
23. damage the cord Never pull on the power cord when removing it from the power outlet When disconnecting the power cord always grasp the attachment plug and not the cord Keep the cord away from liquids heat and sharp edges Replace the power cord if the strain relief or cord insulation is damaged or begins to separate from the attachment plug CAUTION Use only the Welch Allyn USB client cable to connect a laptop computer to the USB client port Any laptop connected to the monitor must be running on a battery a 60601 1 compliant power supply or a 60601 1 compliant isolation transformer Directions for use About warnings and cautions 13 A CAUTION f the touchscreen is not responding properly refer to the troubleshooting section If the problem cannot be resolved discontinue use of the monitor and contact an authorized Welch Allyn service center or qualified service personnel A CAUTION Verify patient identity on the monitor after manual or barcode entry and before printing or transferring patient records 14 About warnings and cautions Welch Allyn Connex Vital Signs Monitor 6000 Series Controls indicators and connectors Note Your model might not contain all of these features Feature Printer Light bar Thermometry Thermometry Thermometry connector behind cover LCD screen Battery compartment behind cover pr Description Optional Printer provides a printout of patient and device
24. e _ To exit the Advanced Settings and return to the Home tab touch Exit Specify server settings 1 Access the Advanced Settings a Touch the Settings tab Touch the Advanced tab b c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the Network tab Touch the Server tab 4 Specify settings Setting Obtain server IP information automatically IP address Port UDP broadcast port Test 5 Do one of the following Action Description Enable the monitor to automatically obtain the server IP information via the network Touch and enter the IP address of the server that is used for patient data communication The range of entry for each field is 0 to 255 Touch and enter the port number associated with the server IP address The range of entry is 0 to 65535 Touch and enter the port number that is used to automatically obtain server IP information The range of entry is 0 to 65535 Touch Test to test the connection to the configured server e Tocontinue in the Advanced Settings touch another tab e To exit the Advanced Settings and return to the Home tab touch Exit 130 Advanced settings Welch Allyn Connex Vital Signs Monitor 6000 Series Service For service related advanced settings see the service manual for this product 131 Troubleshooting This section presents tables of technical alarm and information messages as well as prob
25. important to note the temperature before removing the thermometer probe from the measurement site and then manually record it in the patient record After 10 minutes of using the Direct mode the monitor generates a technical alarm condition and clears the measurement Take a temperature in the Predictive mode A WARNING Inaccurate measurement risk To ensure optimal accuracy always confirm that the correct mode and site are selected A WARNING Patient injury risk Prior to taking a temperature instruct the patient not to bite down on the probe as patient injury and damage to the probe may result A CAUTION Probe covers are disposable nonsterilized and single use Probes are also nonsterilized Do not autoclave probes and probe covers Ensure that probe covers are disposed of according to facility requirements or local regulations 1 Remove the temperature probe from the probe well The monitor sounds a tone as it enters the ready state 2 Insert the probe into a new probe cover and press the probe handle down firmly 3 Touch the Temperature site control E to choose from these measurement sites oral pediatric axillary or adult axillary 4 Hold the probe tip in place at the measurement site For oral temperatures place the probe tip under the patient s tongue on either side of the mouth to reach the sublingual pocket and ask the patient to close his her lips 78 Patient monitoring Welch Allyn Connex Vital Signs Monitor 60
26. in a particular installation If this equipment does cause harmful interference to radio or television reception which can be determined by turning the equipment off and on the user is encouraged to try and correct the interference by one or more of the following measures e Reorient or relocate the receiving antenna e Increase the distance between the equipment and the receiver e Connect the equipment to an outlet on a circuit different from that to which the receiver is connected e Consult the dealer or an experienced radio TV technician for help The user may find the following booklet prepared by the Federal Communications Commission helpful The Interference Handbook This booklet is available from the U S Government Printing Office Washington D C 20402 Stock No 004 000 0034504 Welch Allyn is not responsible for any radio or television interference caused by unauthorized modification of the devices included with this Welch Allyn product or the substitution or attachment of connecting cables and eguipment other than specified by Welch Allyn The correction of interference caused by such unauthorized modification substitution or attachment will be the responsibility of the user Directions for use Standards and compliance 111 Industry Canada IC emissions This device complies with RSS 210 of Industry Canada Operation is subject to the following two conditions 1 this device may not cause interference and
27. information Provides a visual alarm with red and amber LEDs Optional Temperature probe cover box Optional Temperature probe Secures the probe connection to the monitor 1024 x 600 pixels color touchscreen provides a graphical user interface Houses the Li ion battery 16 Controls indicators and connectors Feature Blood pressure Pulse oximetry Feature Power switch and LED Ethernet RJ 45 USB client Nurse call Fan exhaust Ground lug equipotential terminal Power connection Mobile stand mounting hardware Recess for mounting plate Welch Allyn Connex Vital Signs Monitor 6000 Series Description Self contained module for easy replacement Supports dual lumen or single lumen hoses Optional Nellcor Sp02 or Masimo Rainbow SET SpO2 or combined SpO2 SpHb in a self contained module for easy replacement Description Power on Standby switch The LED indicates the charging status when connected to AC power e Green The battery is charged e Amber The battery is charging Provides a hardwired connection to the computer network Provides a connection to an external computer for testing and software upgrades Optional Provides a connection to the hospital nurse call system Not available on the 6300 model Provided for electrical safety testing and as a means for connection of a potential equalization conductor Provides an external AC power connection Secures the
28. mounting plate to the monitor Secures the monitor when mounted on the mobile stand or wall Directions for use Controls indicators and connectors 17 No Feature Description 10 USB connector door Provides access to host USB connections for optional accessories 11 Fanintake 12 Speaker Provides tones A piezo beeper inside the monitor provides backup 18 Controls indicators and connectors Welch Allyn Connex Vital Signs Monitor 6000 Series Setup Supplies and accessories For a list of all approved supplies and accessories see Approved Accessories in the Appendix Insert the battery This procedure applies to first time setup of the monitor A WARNING Risk of fire explosion and burns Do not short circuit crush incinerate or disassemble the battery pack 1 Turn the monitor upside down to access the battery cover 2 Locate the battery cover indicated by O Insert a coin into the slot and push to open Choose a coin that fits comfortably into the slot 4 Slide in the battery 20 Setup Welch Allyn Connex Vital Signs Monitor 6000 Series Note Do not remove the tab label from the battery This tab helps you remove the battery from the compartment when you need to replace it 5 Replace the battery cover by inserting one end into the notched access and then pressing firmly on the opposite end Note New batteries are only 30 percent charged Therefore connect t
29. nurse call Ethernet and USB connectivity The radio is optional 6500 Wireless Includes all Standard features plus an internal 802 11 a b g radio The monitor is covered under the following patents 6 000 846 6 036 361 7 255 475 7 429 245 D480 977 D632 397 and other patents pending For SureTemp Plus configured monitors US patent 6 971 790 applies For Nellcor equipped monitors the following Nellcor US patents and foreign equivalents apply 5 485 847 5 676 141 5 743 263 6 035 223 6 226 539 6 411 833 6 463 310 6 591 123 6 708 049 7 016 715 7 039 538 7 120 479 7 120 480 7 142 142 7 162 288 7 190 985 7 194 293 7 209 774 7 212 847 7 400 919 For Masimo equipped monitors the following Masimo US patents and foreign equivalents apply 5 758 644 5 823 950 6 011 986 6 157 850 6 263 222 6 501 975 7 469 157 and others listed at www masimo com patents htm 108 Specifications Welch Allyn Connex Vital Signs Monitor 6000 Series 109 Standards and compliance General compliance and standards The monitor complies with the following standards 21 CFR Subchapter H Medical Devices US Food and Drug Administration 2002 No 236 Australian Therapeutic Goods Act 93 42 EEC European Economic Community Medical Devices Directive 2007 47 EC European Economic Community Medical Devices Directive 2007 Amendment 94 62 EC European Economic Community Packaging Directive 2002 96 EC Eu
30. on the monitor Verify the patient s pulse rate against the ECG heart rate WARNING Patient injury risk Do not attempt to reprocess recondition or recycle any sensors or patient cables Doing so might damage electrical components WARNING Pulse rate measurement might not detect certain arrhythmias because it is based on the optical detection of a peripheral flow pulse Do not use the pulse oximeter as a replacement or substitute for ECG based arrhythmia analysis WARNING Use the pulse co oximeter as an early warning device As you observe a trend toward patient hypoxemia use laboratory instruments to analyze blood samples to better understand the patient s condition Directions for use Patient monitoring 87 A WARNING The accuracy of SoO2 measurements can be affected by any of the following e elevated levels of total bilirubin e elevated levels of Methemoglobin MetHb e elevated levels of Carboxyhemoglobin COHb e hemoglobin synthesis disorders e low perfusion at the monitored site e the presence of concentrations of some intravascular dyes sufficient to change the patient s usual arterial pigmentation e patient movement e patient conditions such as shivering and smoke inhalation e motion artifact e painted nails e poor oxygen perfusion e hypotension or hypertension e severe vasoconstriction e shock or cardiac arrest e venous pulsations or sudden and significant changes in pulse rate e proximity to an MRI envi
31. open it 2 Detach the accessory s USB cable from USB port on the monitor 3 Close the door and tighten the screw Insert a new roll of paper The printer is located on the top of the monitor Follow these steps to insert the roll of printer paper 1 Grasp the two tabs and pull up to open the printer door 2 Insert a new roll of paper Note The paper roll must be installed as illustrated If the paper roll is not installed correctly the printer will not print properly 3 Advance the end of the roll past the roller so that it extends past the printer door as shown 4 With one hand pull lightly on the paper to take up any slack With the other hand close the printer door by pushing it down and into place until it clicks 26 Setup Welch Allyn Connex Vital Signs Monitor 6000 Series Be certain that the paper does not catch in the printer door Connect AC power You can use the monitor with AC or battery power after charging the battery 1 Insert the power cord into the AC power connector port on the back of the monitor 2 Insert the power plug into a power outlet to power the monitor and to charge the battery Disconnect AC power Disconnect the power plug from the power outlet 27 Startup Power The power button located on the side of the monitor performs the following functions e Powers up the monitor e Sets the monitor into Display power saving mode except
32. power If the integrity of a facility s power or protective earth conductor is in doubt always operate the monitor on battery power alone when it is attached to a patient WARNING Equipment damage and personal injury risk When transporting the monitor on a mobile stand properly secure all patient cables and cords to keep them clear of the wheels and to minimize trip hazards WARNING For operator and patient safety peripheral equipment and accessories that can come in direct patient contact must comply with all applicable safety EMC and regulatory requirements 12 About warnings and cautions A gt Ee D gt D gt p gt Welch Allyn Connex Vital Signs Monitor 6000 Series WARNING All signal input and output I O connectors are intended for connection of only devices complying with IEC 60601 1 or other IEC standards for example IEC 60950 as applicable to the monitor Connecting additional devices to the monitor may increase chassis or patient leakage currents To maintain operator and patient safety consider the requirements of IEC 60601 1 1 Measure the leakage currents to confirm that no electric shock hazard exists WARNING Equipment failure and patient harm risk Do not cover the air intake or exhaust vents on the rear and base of the monitor Covering these vents could cause overheating of the monitor or muffling of alarms WARNING This equipment is not suitable for use in the presence of electro surgery
33. print on interval 4 60 ad 0 Start program intervals Follow these steps to configure the monitor to take automatic NIBP measurements at variable intervals 1 Properly size the blood pressure cuff and position it around the patient s bare upper arm On the Home tab touch ES Select Program Touch the desired program OF de Qood Touch Start intervals Create a new program interval or edit an existing program Follow these steps to create or edit a program interval On the Home tab touch the interval button Bi or E3 Select Program Touch the desired program Touch the keyboard icon and enter the desired program name Enter the desired duration and interval settings Touch Start Intervals e LOL Pe i s The new intervals take effect at the start of the next NIBP measurement Stat intervals You can configure the monitor to take NIBP measurements continuously Directions for use Patient monitoring 71 Intervals Device Clinician Profiles Advanced Q Automatic Q Program A Stat Automatic print on interval Start intervals When you select the Stat option in the Intervals tab the monitor takes repeated NIBP measurements for 5 minutes starting a new cycle each time the cuff deflates below safe venous return pressure SVRP for 2 seconds A WARNING Patient injury risk If you use Stat mode repeatedly periodically observe the patient s limb to ensure that circulation is not impaired and that the cuff
34. printed copy DIR 80016590 Ver D Material Number 720727 80016590 Ver D ps ec rep Regulatory Affairs Representative Welch Allyn Inc riba AL au 4341 State Street Road uba a ar Skaneateles Falls NY 13153 0220 USA TD Navan County Meath www welchallyn com Republic of Ireland Ce MUST gt BRAUN WelchAllyn Advancing Frontline Care Contents INTO UCI em 1 nitended lse ht e ttt datei od SYDD est red ote oY ettet ett 1 ConitraindicatiOn See cotto E Aes retten e dare red 1 Sn TTL TEES 3 Screen elements sariden Ao DASS ER AAA arbatai CIO DRAG RERO DEMERDRESDIPROE 5 About warnings and cautions di YR UY EA 9 General warnings and Cautions eeeeuuee FY YALL LL LLALL LLCC CYLL LL LL DD LL LL DAN 9 Controls indicators and connectors csssessseeeeeeeeeeeeeeeeeeseeeeeeeeeees 15 SOLD a n cee hc ce suelta ftat Du 19 Supplies and accessories ssssssssssssee eene 19 Insert the battery see m b EE RE ERES 19 Mount the monitor on a stand sssssssssssssssssss eee 20 Mount the monitor on the wall iseseisana nna 20 Attach the probe well ssssssssssssee eem emere 20 Attach the temperature probe ssssssssssee Hee 21 Remove the temperature probe and well ssssssssmRRR 22 Connect the NIBP Rose dide ty ERAN EV ARIS E 22 Disconnect the NIBP hose ssssssssssssssssssseeeeeee e emrerennnnnnnnns 23 Connect the SpO2 cable ise it d dicas 23 Disconnect t
35. see Approved Accessories in the Appendix A WARNING Do not rely exclusively on Nurse Call for patient monitoring Although the Nurse Call option enables remote notification of an alarm condition it is not intended to replace appropriate bedside patient monitoring by trained clinicians Note When a patient alarm occurs touching the alarm icon in the Device Status area pauses the alarm tone for a period ranging from 90 seconds to 15 minutes as specified in Advanced settings but the visual alarm indicator s on the monitor and Nurse Call continue 62 Alarms Welch Allyn Connex Vital Signs Monitor 6000 Series 63 Patient monitoring NIBP Noninvasive Blood Pressure NIBP frame From the NIBP frame you can measure blood pressure Located in the upper left corner of the Home tab the NIBP frame contains data and features relevant to noninvasive blood pressure measurement The frame provides different features based on the profile you are using NIBP frame in Monitor profile NIBP frame in Spot Check and Triage profiles NIBP measurement display In all profiles the frame can display systolic and diastolic measurements and MAP calculations You can configure the default view in Advanced settings View indicator Touch the NIBP frame to toggle between views NIBP view 1 NIBP eo displays the SYS DIA measurements as the primary content and the MAP calculation as secondary content 64 Patient monitoring Butt
36. the patient and reapply Reattach the cable to the monitor Sp02 mode only Check sensor or The sensor is operating as an SpO2 only sensor cable because it failed to calibrate properly Remove the sensor from the patient and reapply Sp02 sensor expires in The Sp02 sensor will expire soon Replace the SpO2 sensor Temperature messages Message Possible cause Suggested action Connect temperature probe No probe is connected Connect a temperature probe and retry The probe is faulty Replace the temperature probe The temperature module returned Connect a temperature probe and a connect probe message retry If a probe is already connected replace the probe Insert correct color coded probe well The probe well is missing Insert a temperature probe well Replace temperature probe The probe is faulty Replace the temperature probe Temperature not functional Call for service A module error occurred Call for service The 10 minute timeout for temperature measurement has occurred Temperature time limit exceeded Remove the probe from the measurement site Tissue contact lost The probe has lost contact with the patient s tissue Reposition the probe to restore proper contact with the patient s tissue Retry temperature measurement A probe heater or data error occurred Retry the temperature measurement If the problem persists replace the probe User settings require adjustment Adjust
37. the Advanced settings code d Touch OK The General tab appears displaying the Language tab 2 Select a language 3 Doone ofthe following e _ To continue in the Advanced Settings touch another tab 118 Advanced settings Welch Allyn Connex Vital Signs Monitor 6000 Series e To exit the Advanced Settings and return to the Home tab touch Exit Specify date and time settings 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 On the General tab touch the Date Time tab Specify settings Setting Action Description Date format Select a date format for display Time zone Select your time zone offset from Coordinated Universal Time UTC Automatically adjust clock for daylight saving time Select this to adjust the displayed time by one hour reported by host when the connected host reports daylight savings time Allow users to change date and time Select this to allow clinicians to set the date and time from the Settings tab Display date and time Select this to display the date and time on the Home tab in the Device Status area 4 Doone of the following e To continue in the Advanced Settings touch another tab e To exit the Advanced Settings and return to the Home tab touch Exit Specify advanced alarm settings 1 Access the Advanced Settings a Touch the Settings tab b Touch the
38. the patient s clothing Carefully place the probe in the axilla avoiding contact with other objects or material Always verify direct contact between the probe cover and skin WARNING Patient injury risk When taking rectal temperatures insert the probe tip only 5 8 inch approximately 1 5 cm inside the rectum of adults and only 3 8 inch approximately 1 cm inside the rectum of children to avoid the risk of bowel perforation WARNING Never use a damaged temperature probe The thermometer consists of high quality precision parts and should be protected from severe impact or shock Do not use the thermometer if you notice any signs of damage to the probe or monitor If the thermometer probe is dropped or damaged remove it from use and have it inspected by qualified service personnel CAUTION Inaccurate measurement risk Patient activities such as strenuous exercise ingesting hot or cold liquids eating chewing gum or mints brushing teeth or smoking may affect oral temperature measurements for up to 20 minutes CAUTION Inaccurate measurement risk Always use new probe covers taken from the monitor s probe cover box holder to ensure accurate temperature measurements Probe covers taken from other places or that haven t stabilized in temperature may result in inaccurate temperature measurements Temperature mode selection The monitor with the temperature module takes a patient temperature in either Predictive Normal or Direct mode T
39. the user settings and retry 134 Troubleshooting Message Note This message often accompanies other temperature messages Welch Allyn Connex Vital Signs Monitor 6000 Series Possible cause Suggested action Weight scale messages Message Weight scale not functional Call for service Possible cause The weight scale is not operating properly Suggested action Call for service Message Maximum number of patient records saved Oldest record overwritten Unable to access patient information No data to save Patient ID required to save data Clinician ID required to save data Patient ID required to send data list is full Delete some s to add more Patien pati Stop intervals to select new patient No connection for send Unable to retrieve list Unable to identify clinician Patient data management messages Possible cause The maximum number of patient records in the monitor s memory has been exceeded An error occurred when reading the patient list or patient record during startup No patient da Th da Th da Th da Th Th e con ta igura e con ta igura e con ta igura e maximum a is available ion requires a patient ID to save ion requires a clinician ID to save ion requires a patient ID to send number of patients was exceeded e monitor is set to take interval readings No connectivity i
40. wall mount with channel For a list of approved weight scales and connectivity kits go to www welchallyn com Directions for use Miscellaneous items Part Number BATT69 BATT99 6000 100H 6000 1008 PWCD B PWCD 2 PWCD A PWCD 5 PWCD 4 PWCD 6 PWCD 66 PWCD C PWCD G PWCD 7 PWCD N PWCD 3 PWCD Y PWCD K PWCD T PWCD P PWCD Z 6000 NC 6000 915 6000 915HS 6000 810 4500 925 660 0321 00 Appendix 143 Description Lithium ion battery 6 Cell Lithium ion battery 9 Cell Extended Life Carrying case hard sided Carrying case soft sided Line cord B North America Line cord 2 Europe Line cord A Denmark Line cord 5 Switzerland Line cord 4 United Kingdom Line cord 6 Australia New Zealand Line cord 6 Australia New Zealand Orange Line cord C China Line cord G Argentina Line cord 7 South Africa Line cord N India Line cord 3 Israel Line cord Y Italy Line cord K South Korea Line cord T Taiwan Line cord P Thailand Line cord Z Brazil Nurse Call Cable 2D Barcode scanner kit scanner mounting bracket hardware HS1 M 2D Barcode scanner with coiled USB Mounting Arm for HS1 M Barcode Scanner use with Economy mobile stand with basket only USB cable for wired connectivity Patch cable 50 144 Appendix Part Number 660 0320 00 660 0138 00 715270 6000 50 Service Part Number 1 6000 1 6000 2 S2 6000
41. warnings and cautions A gt D WARNING Many environmental variables including patient physiology and clinical application can affect the accuracy and performance of the monitor The clinician must verify all vital signs information before treating the patient If there is any question about the accuracy of a measurement verify the measurement using another clinically accepted method WARNING Alarm limits are patient or facility specific The clinician must set or verify alarm limits appropriate for each patient Each time the monitor is powered on you must check that the alarm settings are appropriate for your patient before you start monitoring WARNING The monitor is not intended for use during patient transport outside of the medical facility Do not use the monitor to take measurements on any patient in transit WARNING Use only Welch Allyn approved accessories and use them according to the manufacturer s directions for use Using unapproved accessories with the monitor can affect patient and operator safety and can compromise product performance and accuracy WARNING Inaccurate measurement risk Do not connect more than one patient to a monitor 10 About warnings and cautions N Welch Allyn Connex Vital Signs Monitor 6000 Series WARNING Inaccurate measurement risk Dust and particle ingress can affect the accuracy of blood pressure measurements Use the monitor in clean environments to ensure measurement a
42. will return the monitor display to the active state e Touch the screen e Remove the temperature probe from the probe well e Attach the SpO2 sensor to a patient Press Ay Standby The monitor is plugged into a power outlet but the sensors and the display do not operate Note Because power is still available to charge the battery and power the monitor the monitor is in Standby mode The monitor remains in Standby mode until you press Ay Settings for this mode can be changed in the Advanced Settings Display tab Power up the monitor The monitor runs a brief diagnostic self test each time it powers up A WARNING Equipment failure risk The monitor includes a fan that circulates air through the device If the fan does not run when you power up the device remove it from use and inform qualified service personnel immediately Do not use the monitor until the problem is corrected A WARNING To ensure patient safety listen for two audible indicators a piezo beeper and a speaker tone and watch for visual alerts at power up Correct any system errors before using the monitor In addition to the audible indicators the monitor LED light bar illuminates to alert you of alarms Amber indicates a low level alarm Flashing amber indicates a medium level alarm Flashing red indicates a high level alarm A WARNING Always observe the monitor during power up If any display fails to illuminate properly or if an error code displays inform qu
43. 0 mmHg 215 mmHg Pediatric 300 mmHg 215 mmHg Neonate 150 mmHg maximum SureTemp Plus temperature module specifications Temperature range Calibration accuracy 80 F to 1109F 26 7 C to 43 39C 0 2 F 20 19C Direct mode 104 Specifications Welch Allyn Connex Vital Signs Monitor 6000 Series Braun ThermoScan PRO 4000 thermometer specifications refer to manufacturer s directions for use for additional information Temperature range Calibration accuracy 68 F to 1089F 20 C to 42 2 C 0 4 F 20 29C for temperatures ranging from 95 9 F to 107 6 F 35 59C to 42 C e 0 5 F 0 25 C for temperatures outside of this range Display resolution 0 1 F or C Sp02 specifications refer to sensor manufacturer s directions for use for additional information Sp02 performance measurement range Masimo Sp02 sensor accuracy guide Perfusion Pulse rate Saturation Note Saturation accuracy varies by sensor type Nellcor sensor accuracy guide Perfusion Pulse rate Saturation Note Saturation accuracy varies by sensor type 1 to 10096 Accuracy specified when used with Masimo SET pulse oximetry monitors or with licensed Masimo SET pulse oximetry modules using PC series patient cables during no motion Numbers present z 1 standard deviation Plus or minus one standard deviation represents 68 of the population 0 02 to 20 96 25 to 240 beats per minute bpm No motion
44. 00 Series Note Do not hand the probe to patients to place in their mouth For axillary temperatures lift the patient s arm so that the entire axilla is easily seen and place the probe tip as high as possible in the mid axilla Verify that axillary tissue completely surrounds the probe tip and place the arm snugly at the patient s side MS While the measurement is taking place the temperature frame displays the process indicator y A The monitor sounds a tone when the final temperature is reached in approximately 6 to 15 seconds The temperature frame continues to display the temperature in degrees Fahrenheit and degrees Celsius even after the probe is returned to the probe well TEMPERATURE 97 9 F 36 69C Note To switch to the Direct mode touch E after you acquire the Predictive mode measurement The temperature frame in the lower left corner changes to MODE Direct as it switches to the Direct mode The monitor sounds a tone at the start of a Direct mode measurement Remove the probe after the temperature measurement is complete and firmly press the eject button on the top of the probe to release the probe cover Directions for use Patient monitoring 79 A WARNING Patient injury risk Do not exceed the recommended temperature measurement durations in Direct mode Continuous measurement durations of 3 minutes at the oral and rectal sites and 5 minutes at the axillary site are recommend
45. 11a g 6Mbps or higher during vitals transmission only approximately 2 seconds per reading US FCC Part 15 Class B C UL CE 47 CFR Part 2 1093 15 207 15 209 15 247 15 407 FCC OET Bulletin 65C Europe CE EN 50371 EN ETSI 300 328 V1 7 1 301 489 1 V1 6 1 301 489 17 V1 2 1 301 893 V1 4 1 Canada RSS 210 RSS GEN RSS 102 Hong Kong HKTA 1039 UDP DHCP TCP IP UDP TCP IP OFDM 802 11a g DSSS CCK 802 115 40mW typical country dependent 802 11e 802 11h 802 111 802 11X Channel restrictions in the 5 GHz band are determined by country Marking by the symbol indicates that usage restrictions apply To ensure compliance with local regulations be sure the correct country in which the access point is installed is selected This product can be used with the following restriction s France Outdoor use is limited to 10 mW EIRP within the band 2454 to 2483 5 MHz Note Effective Isotropic Radiated Power EIRP Note Some countries restrict the use of 5 GHz bands The 802 11a radio in the monitor uses only the channels indicated by the access point with which the radio associates The hospital IT department must configure access points to operate with approved domains Configuration options The monitor is available in multiple configurations Directions for use Patents Specifications 107 Model Description 6300 Basic Includes USB connectivity Ethernet connectivity is optional 6400 Standard Includes
46. 2 this device must accept any interference including interference that may cause undesired operation of this device L utilisation de ce dispositif est autoris e seulement aux conditions suivantes 1 il ne doit pas produire de brouillage et 2 utilisateur du dispositif doit tre pr t accepter tout brouillage radio lectrique recu m me si ce brouillage est susceptible de compromettre le fonctionnement du dispositif This Class B digital apparatus complies with Canadian ICES 003 Cet appareil num rique de la classe B est conform la norme NMB 003 du Canada European Union Czech Danish Dutch English Estonian Finnish French German Greek Hungarian Italian Latvian Lithuanian Welch Allyn t mto prohla uje ze tento RLAN device je ve shod se z kladn mi po adavky a dal mi p slu n mi ustanoven mi sm rnice 1999 5 ES Undertegnede Welch Allyn erkl rer herved at f lgende udstyr RLAN device overholder de v sentlige krav og vrige relevante krav i direktiv 1999 5 EF Bij deze verklaart Welch Allyn dat deze RLAN device voldoet aan de essenti le eisen en aan de overige relevante bepalingen van Richtlijn 1999 5 EC Hereby Welch Allyn declares that this RLAN device is in compliance with the essential requirements and other relevant provisions of Directive 1999 5 EC K esolevaga kinnitab Welch Allyn seadme RLAN device vastavust direktiivi 1999 5 EU p hin uetele ja nimetatud di
47. 20 Soft 12L Disposable Cuff soft LG AD LONG 2 tube box of 20 Soft 13 Disposable Cuff soft THIGH 2 tube box of 20 5082 101 1 Disposable Neo 1 disposable cuff male luer connector box of 10 cuffs 140 Appendix Part Number 5082 102 1 5082 103 1 5082 104 1 5082 105 1 008 0851 00 Model Disposable Disposable Disposable Disposable Disposable Welch Allyn Connex Vital Signs Monitor 6000 Series Description Neo 2 disposable cuff male luer connector box of 10 cuffs Neo 3 disposable cuff male luer connector box of 10 cuffs Neo 4 disposable cuff male luer connector box of 10 cuffs Neo 5 disposable cuff male luer connector box of 10 cuffs Neonatal Cuff Kit 1 each neo 1 5 reusable infant cuff NIBP hose Blood pressure accessories Latex free Part Number 4500 30 4500 31 4500 32 6000 30 6000 31 6000 33 5200 08 Model SureBP SureBP SureBP BP BP BP Description Double tube blood pressure hose 5 ft Double tube blood pressure hose 10 ft Double tube blood pressure hose 8 ft Single tube blood pressure hose 5 ft Single tube blood pressure hose 10 ft Neonatal blood pressure hose 10 ft Calibration T connector Masimo pulse oximetry for use with devices with SpO2 Part Number LNCS DCI LNCS DCIP LNCS ADTX LNCS PDTX RED LNC 10 LNCS YI LNCS TC I LNCS Neo L 3 Neo Wrap RP LNCS Inf 3 Model LNC
48. 42 EEC Manufacturer Reorder number Do not reuse Nonionizing electromagnetic radiation Restrictions for use of wireless device in Europe European Community s Class 2 radio eguipment Welch Allyn Connex Vital Signs Monitor 6000 Series A SN 9 E Va AC input power Ethernet RJ 45 Nurse call European Community Representative Defibrillation proof Type BF applied parts Serial number China RoHS markings for control of pollution caused by electronic information products XX indicates Environmentally Friendly Use Period in years Recycle the product separate from other disposables Call for maintenance Screen elements Global navigation Select option YA O NIBP NIBP start NIBP stop STOP Intervals status indicators Lc NIBP view toggle Temperature Process indicator Temperature site control Direct mode selector 6 Screen elements Welch Allyn Connex Vital Signs Monitor 6000 Series Sp02 and Pulse rate SatSeconds timer Nellcor feature only Pulse amplitude bar EZ SpO2 view toggle Response mode selector AN touch for Fast mode Heart rate in beats per EZ minute Total hemoglobin SpHb SpHbv SpHb view toggle vvv Averaging selector Manual parameters Manual parameter selector HEIGHT WEIGHT PAIN Alarm and information messages Alarm limit button o Alarm On Off toggle Multiple alarms toggle Alarm audio pa
49. AAMI SP10 2002 standard as children 28 days or less of age if born at term 37 weeks gestation or more otherwise up to 44 gestational weeks CAUTION Correct sizing of the blood pressure cuff is important for accurate blood pressure readings A cuff that is too small might provide false high readings while a cuff that is too large might provide false low readings The monitor uses the oscillometric method to determine blood pressure therefore if the cuff extends to the antecubital fossa bend in the elbow you can still acguire an accurate blood pressure reading Before taking an NIBP measurement follow these steps to select the appropriate cuff for the patient 1 Measure the circumference of the patient s bare upper arm midway between the elbow and shoulder 2 Choose the appropriate cuff size based on the circumference measurement If the circumference of the patient s arm falls between two cuff sizes use the larger cuff size 3 Wrap the cuff around the patient s bare upper arm and verify that the artery index marker lies somewhere between the two range markings on the cuff Cuff measurements The following tables provide measurements for Welch Allyn blood pressure cuffs One piece cuff measurements Cuff Size Infant Small child Child Small adult Adult Large adult Thigh Neonatal soft disposable cuffs with male Luer slips Cuff Size NEO 1 Circumference cm 9 0 13 0 12 0 16 15 0 21
50. Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears Touch the Alarms tab Specify settings Setting Action Description Allow user to disable alarms Select to allow clinicians to turn off or turn on all alarm limits for each vital sign The control is on each parameter specific tab on the Alarms tab Allow user to turn off general audio Select to allow clinicians to turn off all audio notification for alarms This control is on the Alarms tab on the General tab Directions for use Minimum alarm volume Nurse call threshold Audio pause time Sp02 alarm condition delay SpHb alarm condition delay 4 Do one of the following Advanced settings 119 Select the minimum alarm volume available If you select High then Medium and Low are not available to the clinician These controls are on the Alarms tab on the General tab Select the minimum priority alarm that activates a nurse call relay If you select High only high level alarms activate a nurse call relay Specify the amount of pause time that is added to the 60 second pause time When a clinician pauses an audio alarm tone the tone is paused for the combined amount of time Specify the minimum amount of time that an SpO2 alarm condition must be active before audio and visual signals occur SatSeconds is available with Nellcor SpO2 sensors If you select 0 seconds or 10 seconds SatSeconds is disabled and it is remo
51. K button Description Displays the characters you enter When touched removes the rightmost character from the data field When touched enters a space in the data field When touched enters the next letter as uppercase When touched returns to the primary keyboard layout The keyboard changes from normal layout when you touch one of these e The symbols key e The diacritical marks key When touched the keyboard displays symbols The keyboard returns to its normal layout when you touch one of these e Any symbol e The letters key e The symbols key Note The symbols that display match the selected language When touched the keyboard displays letters with diacritical marks The keyboard returns to its normal layout when you touch one of these e Any letter e The letters key e The diacritical marks key Note This key appears only when the selected language uses diacritical marks When touched accepts the entry for the current field then clears the field to allow data entry for the next field When touched the keyboard disappears and the content of the data field remains the same When touched the keyboard disappears and the entered characters appear in the data field 44 Using the keypad keyboard and barcode scanner Welch Allyn Connex Vital Signs Monitor 6000 Series Enter a letter or number 1 With the keyboard open touch letters or numbers 2 Do one of the following e T
52. S LNCS LNCS LNCS LNCS LNCS LNCS LNCS LNCS LNCS Description Reusable finger sensor Adult Reusable finger sensor Pediatric Disposable adhesive finger sensor Adult 20 per case Disposable adhesive finger sensor Pediatric 20 per case 10 foot cable with sensor connector Multisite reusable sensor 1 sensor 6 adhesive wraps Reusable ear sensor Disposable adhesive finger sensor Neonate Adult 20 per case Replacement wrap for neonatal adhesives 100 per case Disposable adhesive finger sensor Infant 20 per case Directions for use Part Number Inf Wrap RP YI AD YI FM Model LNCS LNCS LNCS Appendix 141 Description Replacement wrap for infant adhesives 100 per case Multisite adhesive wrap adult pediatric neonatal for YI sensor 100 per case Multisite foam wrap adult pediatric neonatal for YI sensor 12 per case Masimo Rainbow SET for use with devices with SpO2 and SpHb Part Number Model Description 104220 Rainbow Adult reusable sensor and 3 foot cable 104360 Rainbow ReSposable R2 25 sample pack 104149 Rainbow Extension cable 20 pin 12 feet Nellcor pulse oximetry Part Number Model Description DS 100A OxiMax Durasensor adult oxygen transducer DOC 10 OxiMax Extension cable 10 feet DOC 8 OxiMax Extension cable 8 feet DOC 4 OxiMax Extension cable 4 feet D YS OxiMax Dura Y oxygen transducer 1 sensor 40 wraps D YSE OxiMax Ear clip u
53. Welch Allyn Connex Vital Signs Monitor 6000 Series J WY 2 M a TTY ETT De Directions for use Software versions 1 0X 1 7X WelchAllyn Advancing Frontline Care 2013 Welch Allyn All rights are reserved To support the intended use of the product described in this publication the purchaser of the product is permitted to copy this publication for internal distribution only from the media provided by Welch Allyn No other use reproduction or distribution of this publication or any part of it is permitted without written permission from Welch Allyn Welch Allyn assumes no responsibility for any injury to anyone or for any illegal or improper use of the product that may result from failure to use this product in accordance with the instructions cautions warnings or statement of intended use published in this manual Welch Allyn Connex SureTemp FlexiPort and SureBP are registered trademarks of Welch Allyn Vital Signs Monitor 6000 Series is a trademark of Welch Allyn LNCS SpHb ReSposable and Rainbow are trademarks of and SET LNOP and Masimo are registered trademarks of Masimo Corporation Possession or purchase of a Masimo SpO2 or Masimo SpHb equipped device does not convey any express or implied license to use the device with unauthorized sensors or cables which would alone or in combination with this device fall within the scope of one or more of the patents relating to this device Nell
54. adhesive Attach the sensor to the patient according to the manufacturer s directions for use observing all warnings and cautions Note If a sterile sensor is required select a sensor that has been validated for sterilization and follow the sensor manufacturer s directions for sterilizing the sensor Place the sensor and the NIBP cuff on different limbs to reduce unnecessary alarms when you monitor these parameters at the same time Note A range of sensors is available for different patient sizes and measurement sites Consult the sensor manufacturer s instructions for selecting the correct sensor Confirm that the monitor displays SpHb or SpHbv data within 160 seconds of connection to the patient A WARNING Patient injury risk Incorrect sensor application or excessive duration of sensor use can cause tissue damage Inspect the sensor site periodically as directed in the sensor manufacturer s instructions While SpHb is being measured the displayed SpO2 and pulse rate are derived from the same sensor If SpO2 is not available the pulse rate is derived from NIBP Detaching the sensor during a measurement triggers an alarm If SpHb is being measured continuously on a patient for an extended period change the sensor location at least every three hours or as indicated by the sensor manufacturer s instructions Configure SpHb alarms Follow these steps to set alarm limits for SpHb measurements DUO NN Verify that you are us
55. age Possible cause Suggested action Set date and time The date or time is not set Set the date and time The date or time is not set properly Reset the date or time Ambient temperature outside The ambient temperature is out of range Operate the monitor within the operating range Retry specified temperature range measurement Retry patient temperature measurement If the message persists move the patient and the monitor to a cooler location Device shutdown is not available Device cannot perform an immediate shutdown Touch OK wait and retry at this time Advanced settings unavailable Sensors are taking measurements Stop continuous measurements A physiological alarm condition is active Respond to or reset the alarm Spot Check measurements have not been saved Save the measurements Unable to load language Chinese did not load Power down and restart the monitor Unexpected restart occurred Call A system error caused the monitor to restart Call for service for service Message Possible cause Suggested action Low battery 5 minutes or less Battery power is extremely low Connect the monitor to AC remaining High priority alarm power If not connected to AC power the monitor powers down when AC power is depleted Low battery 30 minutes or less Battery power is low Touch the alarm icon to dismiss remaining or connect the monitor to AC power Powering down Call for service Power manager or battery faults have occu
56. al might not apply Before using the monitor read the sections of the manual that pertain to your use of the monitor Intended use The VSM 6000 Series of monitors is intended to be used by clinicians and medically qualified personnel for monitoring of neonatal pediatric and adult patients for e noninvasive blood pressure e pulse rate e noninvasive functional oxygen saturation of arteriolar hemoglobin SpO2 and e body temperature in normal and axillary modes The most likely locations for patients to be monitored are general medical and surgical floors general hospital and alternate care environments The optional Masimo Rainbow SET and accessories are indicated for the continuous noninvasive monitoring of total hemoglobin concentration of adult pediatric and neonatal patients during both motion and no motion conditions and for patients who are well or poorly perfused in hospitals and hospital type facilities Optional compatible weight scales e g Health o meter can be used for height weight and BMI input This product is available for sale only upon the order of a physician or licensed health care professional Contraindications This system is not intended to be used e on patients connected to heart lung machines e on patients being transported outside a healthcare facility nearan MRI machine e ina hyperbaric chamber 2 Introduction Welch Allyn Connex Vital Signs Monitor 6000 Series e near fla
57. al time measurements over a user selected period In Advanced settings you can select the period displayed The graph shows total hemoglobin level on the y axis and time on the x axis oldest measurements on the left to newest measurements on the right The entire graph updates every 10 seconds To the right of the graph the frame displays the current measurement in numeric format 90 Patient monitoring Measure SpHb gt gt Pe Welch Allyn Connex Vital Signs Monitor 6000 Series WARNING Inaccurate measurement risk Use only Masimo Rainbow SET sensors and accessories on Masimo equipped monitors WARNING The pulsations from intra aortic balloon support can increase the pulse rate displayed on the monitor Verify the patient s pulse rate against the ECG heart rate WARNING Patient injury risk Do not attempt to reprocess recondition or recycle any sensors or patient cables Doing so might damage electrical components WARNING Pulse rate measurement might not detect certain arrhythmias because it is based on the optical detection of a peripheral flow pulse Do not use the pulse oximeter as a replacement or substitute for ECG based arrhythmia analysis WARNING Use the pulse co oximeter as an early warning device As you observe a trend toward patient hypoxemia use laboratory instruments to analyze blood samples to better understand the patient s condition WARNING The accuracy of SpHb measurements can be affe
58. alarms e Constant amber for low priority alarms Home tab AN Alarm limit exceeded SpO2 LOW TEMPERATURE 98 1 F 36 7 C PATIENT HEIGHT WEIGHT PAIN 13579 72 0 1971 3 Home tab notifications Notification Description Device Status area The area changes color and displays a message with an accompanying status icon or button If the alarm tone is in a pause interval a timer countdown appears If multiple alarms and information messages are active the Device Status area shows the highest priority alarm If the alarms are equal in priority the most recent alarm message appears You can cycle through the messages for each active alarm Parameter frame The background color changes Touch this area to pause or turn off an alarm audio tone Visual indicators and Nurse Call notification will persist during an audio paused condition Alarm Limit control The icon in this control indicates the status of the alarm limit settings Red and amber icons indicate measurements that have exceeded alarm limits Touch this control to navigate to a parameter specific tab where you can modify alarm limit settings Icons on the Home tab Icons in parameter frames The icons in the parameter frames indicate alarm notification settings When alarm limits are on the icons will be black and white until an alarm occurs Then the icons will change color to indicate the priority of the alarm Red icons represent high priority alarms and
59. alified service personnel immediately or call your nearest Welch Allyn Customer Service or Technical Support facility Do not use the monitor until the problem is corrected CAUTION Always use the monitor with an adequately charged and properly functioning battery For continuous monitoring always connect to AC power D CAUTION Use only a Class grounded AC power cord for powering this monitor D Directions for use Startup 29 Press K to power up the monitor Following a successful self test the monitor displays the Welch Allyn logo the LED light bar located on the handle flashes and a power up tone sounds The startup screen then appears with the following banner across the bottom WelchAllyn Connex If a system error is detected the monitor becomes inactive until you press Ay Or until the monitor shuts down automatically The monitor displays a system fault message that contains a wrench icon A and a system fault code to aid service personnel and engineers in diagnosing the problem Power down the monitor 1 Touch the Settings tab 2 Touch the Device tab 3 Touch Power down This power down method which places the monitor into Standby mode ensures that patient measurements are retained in the monitor memory for a maximum of 24 hours These saved measurements are avallable for recall printing or to send electronically to the network This method also ensures that any configuration settings you ha
60. all 25 V AC or 60 V DC maximum at 1A maximum Directions for use NIBP specifications Cuff pressure range Systolic range Diastolic range Cuff Inflation Target Maximum Target Pressure Blood pressure determination time Blood pressure accuracy Mean Arterial Pressure MAP range The formula used to calculate MAP yields an approximate value Pulse rate range using blood pressure determination Pulse rate accuracy using blood pressure determination Overpressure cutoff Specifications 103 Meets or exceeds ANSI AAMI SP10 2002 standards for cuff pressure range Adult 30 to 260 mmHg StepBP SureBP Pediatric 30 to 260 mmHg StepBP SureBP Neonate 20 to 120 mmHg StepBP Adult 20 to 220 mmHg StepBP SureBP Pediatric 20 to 220 mmHg StepBP SureBP Neonate 10 to 110 mmHg StepBP Adult 160 mmHg StepBP Pediatric 120 mmHg StepBP Neonate 90 mmHg StepBP Adult 280 mmHg StepBP SureBP Pediatric 280 mmHg StepBP SureBP Neonate 130 mmHg StepBP Typical 15 seconds Maximum 150 seconds Meets or exceeds ANSI AAMI SP10 2002 standards for noninvasive blood pressure accuracy 25 mmHg mean error 8 mmHg standard deviation Adult 23 to 230 mmHg StepBP SureBP Pediatric 23 to 230 mmHg StepBP SureBP Neonate 13 to 110 mmHg StepBP Adult 30 to 200 bpm StepBP SureBP Pediatric 30 to 200 bpm StepBP SureBP Neonate 35 to 220 bpm StepBP 45 090 3 bpm Adult 30
61. amber icons represent medium or low priority alarms Directions for use Alarms 55 Icons in parameter frames Name and status Alarm off No visual or audio alarms or Nurse Call notification will occur for this parameter Alarm on Audio and visual notifications and Nurse Call are enabled Alarm audio off Only visual notifications including Nurse Call will occur m Alarm audio paused The audio tone is paused for a period ranging from 90 seconds to 15 minutes The icon remains until the paused time counts down to 0 gt Icons in the Device Status area The icons in the Device Status area are black and white but the background area changes colors to indicate the alarm priority Messages accompany these icons These icons can be controls or status indicators Icons in the Device Status area Icon Name and status Alarm active One or more alarms are active Touch this icon to pause or turn off the audio tone Alarm audio off Audio signals are disabled but alarm limits and visual alarm signals remain active Multiple alarms toggle Touch this icon to cycle through the messages for each active alarm D gt 2 amp Alarm audio paused The audio tone is paused for a period ranging from 90 seconds to 15 minutes The icon remains until the paused time counts down to 0 Touch this icon to reset the pause interval The pause interval is determined by settings in the Advanced tab gt
62. anual Height Weight Pain Respiration in Ib bpm 94 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series 3345097245 4A West 14 24 List Summary Modifiers Manual Height Weight Pain aeu 191 7 aeu 3 afa gt 2 Zu Zu 72 0 2 Touch the up down arrow keys or the keypad to manually adjust height weight pain level temperature respiration rate or other parameters Note If an approved battery powered weight scale is attached to the monitor measurements from the weight scale populate fields in the Manual tab You can adjust weight and height measurements on this tab but if you do the read only BMI field will clear Note Ensure that the current patient ID is correct before saving 3 Touch mope to confirm settings and return to the Home tab Note During intervals each automatic and manual save of patient measurements clears all measurements from the Manual parameters frame 95 Maintenance and service Perform periodic checks Welch Allyn recommends that each facility conduct periodic checks of each monitor 1 Check the following at least daily Audio speaker and piezo beeper tones especially at startup Fan especially at startup Touchscreen alignment Date Time 2 Visually inspect the following at least weekly the monitor for any damage or contamination all cables cords and connector ends for damage or contamination all mechanical parts including
63. are compatible with the monitor e 70 percent isopropyl alcohol e 10 percent chlorine bleach solution Directions for use Maintenance and service 99 Note Disinfect according to your facility s protocols and standards or local regulations 70 percent isopropyl alcohol Wipe the monitor with a clean cloth slightly dampened with 70 percent isopropyl alcohol 10 percent chlorine bleach solution 1 Wipe the monitor with a clean cloth slightly dampened with a 10 percent bleach and water solution Follow the cleaning agent manufacturer s guidelines 2 Rinse with a clean cloth slightly dampened with water that meets EP and USP guality standards 3 Allow the monitor surface to dry for a minimum of 10 minutes before using the monitor Clean the accessories 1 Wipe the NIBP hose and any reusable cuffs with a damp cloth moistened in a mild detergent solution 2 Wipe the temperature probe with a cloth dampened with alcohol warm water or an appropriately diluted nonstaining disinfectant solution 3 Clean the pulse oximetry sensors with a cloth dampened with 70 percent isopropyl alcohol or 10 percent chlorine bleach solution Clean the ear thermometer according to the manufacturer s directions for use 5 Clean the ear thermometer dock with the same cleaning agents used on the monitor A CAUTION Never immerse any monitor accessories Clean the stand The same cleaning agents used on the monitor can be used on the stand and
64. atteries in refuse containers Always recycle batteries according to local regulations WARNING Electric shock hazard Do not open the monitor or attempt repairs The monitor has no user serviceable internal parts Only perform routine cleaning and maintenance procedures specifically described in this manual Inspection and servicing of internal parts shall only be performed by qualified service personnel WARNING Inaccurate measurement risk Do not expose to temperatures higher than 122 F 50 C WARNING Inaccurate measurement risk Do not use the monitor on patients who are on heart lung machines WARNING Use the monitor only as described in this directions for use Do not use the monitor on patients as described in the Contraindications WARNING Inaccurate measurement risk Do not use the monitor on patients who are experiencing convulsions or tremors WARNING Wall mounted equipment and accessories must be installed in accordance with accompanying instructions Welch Allyn is not responsible for the integrity of any installation not performed by authorized Welch Allyn service personnel Contact an authorized Welch Allyn service representative or other qualified service personnel to ensure professional installation for safety and reliability of any mounting accessory WARNING Do not place the monitor in any position that might cause it to fall on the patient WARNING Welch Allyn is not responsible for the integrity of a facility s
65. ccuracy If you notice dust or lint build up on the monitor s vent openings have the monitor inspected and cleaned by a qualified service technician WARNING Liquids can damage electronics inside the monitor Prevent liquids from spilling on the monitor If liquids are spilled on the monitor Power down the monitor Disconnect the power plug Remove battery pack from the monitor Dry off excess liquid from the monitor pU c Note If liquids possibly entered the monitor remove the monitor from use until it has been properly dried inspected and tested by qualified service personnel or Reinstall battery pack 6 Power on the monitor and verify that the monitor functions normally before using it If liquids enter the printer housing 1 Power down the monitor 2 Disconnect the power plug 3 Remove battery pack from the monitor 4 Remove and discard the paper roll 5 Clean and dry the inside of the printer housing Note The printer housing has a drain tube that directs liquids down and out the bottom of the monitor If liquids possibly entered other openings in the monitor remove the monitor from use until it has been properly dried inspected and tested by qualified service personnel 6 Install a new roll of paper 7 Power on the monitor and verify that the monitor functions normally before using it WARNING Safety risk Damaged cords cables and accessories can affect patient and operator safety Never l
66. cor and OxiMax are registered trademarks of Nellcor Puritan Bennett Inc Braun and ThermoScan are registered trademarks of Braun GmbH Health o meter is a registered trademark of Sunbeam Products Inc used under license Software in this product is Copyright 2013 Welch Allyn or its vendors All rights are reserved The software is protected by United States of America copyright laws and international treaty provisions applicable worldwide Under such laws the licensee is entitled to use the copy of the software incorporated with this instrument as intended in the operation of the product in which it is embedded The software may not be copied decompiled reverse engineered disassembled or otherwise reduced to human perceivable form This is not a sale of the software or any copy of the software all right title and ownership of the software remain with Welch Allyn or its vendors For information about any Welch Allyn product call Welch Allyn Technical Support USA 1 800 535 6663 Australia 61 2 9638 3000 1 315 685 4560 Canada 1 800 561 8797 China 86 21 6327 9631 European Call Center 353 46 90 67790 France 33 155 69 58 49 Germany 49 695 098 5132 Italy 39 026 968 2425 Japan 81 42 703 6084 Latin America 1 305 669 9003 Malaysia 603 7875 3341 Netherlands 31 202 061 360 Singapore 465 6419 8100 South Africa 27 11 777 7555 Spain 34 917 499 357 Sweden 46 85 853 6551 United Kingdom 44 207 365 6780 103730 CD 103501
67. covers for integrity all safety related labeling for legibility and adhesion to the monitor all accessories cuffs tubing probes sensors for wear or damage documentation for current revision of the monitor 3 Visually inspect the following at least monthly Mobile stand wheels for wear and faulty operation Mounting screws on wall or cart for looseness and wear Update settings replace items or call for service as necessary based on results of visual inspection Do not use the monitor if you see any signs of damage Qualified service personnel must check any monitor that is damaged for proper operation before putting the monitor back into use Replace the printer paper The printer is located on the top of the monitor Follow these steps to replace the roll of printer paper 1 Grasp the two tabs and pull up to open the printer door 2 Remove the empty core 96 Maintenance and service Welch Allyn Connex Vital Signs Monitor 6000 Series A warnine Hot surface Do not touch the printer mechanism 3 Insert a new roll of paper Note The paper roll must be installed as illustrated If the paper roll is not installed correctly the printer will not print properly 4 Advance the end of the roll past the roller so that it extends past the printer door as shown 5 With one hand pull lightly on the paper to take up any slack With the other hand close the printer door by pushing it down and into place until it click
68. cted by any of the following e elevated levels of total bilirubin e elevated levels of Methemoglobin MetHb e elevated levels of Carboxyhemoglobin COHb e hemoglobin synthesis disorders e low perfusion at the monitored site e the presence of concentrations of some intravascular dyes sufficient to change the patient s usual arterial pigmentation e patient movement e patient conditions such as shivering and smoke inhalation e motion artifact e painted nails e poor oxygen perfusion e hypotension or hypertension e Severe vasoconstriction e shock or cardiac arrest e venous pulsations or sudden and significant changes in pulse rate e proximity to an MRI environment e moisture in the sensor e excessive ambient light especially fluorescent e the use of the wrong sensor e _ a sensor applied too tightly 1 Verify that the sensor cable is connected to the monitor Directions for use Patient monitoring 91 A WARNING Patient injury risk The sensor and extension cable are intended only for connection to pulse co oximetry equipment Do not attempt to connect these cables to a PC or any similar device Always follow the sensor manufacturer s directions for care and use of the sensor Verify that you are using the Monitor profile Clean the application site Remove anything such as nail polish that could interfere with sensor operation Note Do not use disposable sensors on patients who have allergic reactions to the
69. ds Add a patient to the patient list Note If the monitor is configured to retrieve the patient list from the network 1 2 you cannot manually add a patient to the patient list Touch the Patients tab Touch Add Touch and then enter patient information Touch UED to cycle through the patient data fields Note You can use a barcode scanner to enter a patient ID in the Patient ID field Touch 9 in the Patient ID field scan the barcode and touch OK Touch OK to return to the Home tab The information is saved A CAUTION Verify patient identity on the monitor after manual or barcode entry and before printing or transferring patient records Load patient data with the barcode scanner You can use a barcode scanner to query existing patient records and perform an ADT patient name match 48 Patient data management Welch Allyn Connex Vital Signs Monitor 6000 Series Note If the monitor is connected to the network the monitor can receive a patient name from patient records associated with a scanned ID number 1 Ensure that you are on the Home tab 2 Scan the patient s barcode with the barcode scanner The Patient ID appears in the Patient frame A CAUTION Verify patient identity on the monitor after manual or barcode entry and before printing or transferring patient records Select a patient Touch the Patients tab 2 If the monitor is connected to the network touch Retrieve list on the List tab
70. ds alarm management The SatSeconds feature is an SpO2 alarm management system available only with monitors that are equipped with Nellcor OxiMax Technology The SatSeconds feature is the product of the time and magnitude that a patient falls outside of the SpO2 alarm limits For example three points below the alarm limit for 10 seconds equals 30 SatSeconds An alarm is triggered only when a desaturation event reaches the SatSeconds limit The SatSeconds feature is clinician controlled and can be set to 0 10 25 50 or 100 SatSeconds If a desaturation event resolves on its own within the preset time the clock will automatically reset and the monitor will not alarm 86 Patient monitoring 25 Note SpO2 waveform view Welch Allyn Connex Vital Signs Monitor 6000 Series The SatSeconds feature has a built in safety protocol that sounds an alarm whenever three SpO2 violations of any amount or duration occur within a 1 minute period The waveform view shows the real time SpO2 plethysmograph waveform You can select the waveform sweep speed in Advanced settings Measure Sp02 and pulse rate gt Cb BP PPP WARNING Inaccurate measurement risk Use only Masimo Rainbow SET sensors and accessories on Masimo equipped monitors WARNING Inaccurate measurement risk Use only Nellcor sensors and accessories on Nellcor equipped monitors WARNING The pulsations from intra aortic balloon support can increase the pulse rate displayed
71. dvanced Settings and return to the Home tab touch Exit Specify the manual parameters The Manual Parameters frame is in the lower right corner of the Home tab You can manually enter values for parameters in the frame You also can specify which parameters appear in the frame 1 Access the Advanced Settings a b C d Touch the Settings tab Touch the Advanced tab Enter the Advanced settings code Touch OK The General tab appears 2 Touch the Parameters tab 3 Touch the Manual tab Directions for use Advanced settings 125 Fil Advanced Settings y Exit NIBP Temperature Spo2 SpHb Pulse rate Manual Display Y Height Qa 0 1 Y Bm JS Weight O J Pain RR 4 Select up to four parameters and associated units of measure for display in the Manual Parameters frame If the monitor has the SureTemp Plus temperature module the Temperature parameter is not available here or in the Manual Parameters frame 5 Doone of the following To continue in the Advanced Settings touch another tab To exit the Advanced Settings and return to the Home tab touch Exit Data management Specify patient ID settings Patient identification appears on the Home tab in the Patient frame and it is listed in various tabs such as the Patient tab and the Review tab 1 2 3 4 Access the Advanced Settings a b C d Touch the Settings tab Touch the Advanced tab Enter the Advanced
72. e Communications module did not Communication failure Call for service power on properly Power down the device High priority alarm Ethernet messages Possible cause Message Network not found check network A network cable is unplugged cable connection Suggested action Check the network cable connection If problem persists A network connection is broken elsewhere call for service USB messages Message Possible cause Suggested action USB Communication failure Call An internal or external device is connected but Power down and restart for service failed enumeration Check USB connections If problem persists call for service External device not licensed for A license for an external device e g barcode Disconnect the unlicensed use scanner has not been activated device Call for service to obtain the authorization code from Welch Allyn to activate the license Disconnect the unrecognized device External device not recognized An unrecognized external device is connected Incompatible Welch Allyn device A communication protocol failure has occurred Call for service 136 Troubleshooting Welch Allyn Connex Vital Signs Monitor 6000 Series Message Possible cause Suggested action USB accessory disconnected The USB cable between an external device and Confirm that the USB cable is the monitor is disconnected connected to the device and the monitor System messages Mess
73. e Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the Other tab 3 In the Location ID box touch mn and enter up to 20 alphanumeric characters 4 Doone ofthe following e _ To continue in the Advanced Settings touch another tab e _ To exit the Advanced Settings and return to the Home tab touch Exit Enable monitor profile changes You can allow clinicians to change the active profile on the monitor Available profiles are Monitor Spot Check and Triage When this option is enabled clinicians can change the name of the profile as well 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the Other tab 3 Select Allow profile change 4 Do one of the following e _ To continue in the Advanced Settings touch another tab e _ To exit the Advanced Settings and return to the Home tab touch Exit Specify power line freguency 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the Other tab Directions for use Advanced settings 121 3 Select the power line frequency for AC power supplied to the monitor 4 Do one of the following e _ To continue in the Advanced Settings touch another tab e _ To exit the Advanced Settings and retur
74. e eic t d en eie d 92 Manual parameters frame reniei saae eee eem eene 93 Maintenance and service riirii rc oeieo nennen nnn DD nnn 95 Perform periodic CHECKS anes is 95 Replace the printer paper ciresarii ree ia eem emen 95 Change the Daen x decer tt AA d as 97 Cleanse YO terrse tete eine thes Lied ertet E n eh O eg PU OE GY 98 Clean the accessories sssssssssese LL LL LL mene rrernes LL FF srt ns sells leis 99 Directions for use Contents v Cle AMINE stand ee qe et ete tet Naat eae aa o 99 SOL Uds y o y POCA O tens Y YO O O ie I HN HWNW E IUE EE 101 Physical Specific Sii tette ceret t ag tr FE 101 Environmental specifications sekis e a a ee eene nennen 105 Monitor radio Rt v Y cine Tents clan e e tian a Sc ee 105 GontigutetioncODtIOFis i e Pre EO EM TOT Aine ee 106 Patents uote Ep E Ete id es 107 Standards and compliance minis 109 General compliance and standards ssssssssssseeeee Fan 109 General radio COMPlIA CE redeat diee e edere eder ae 110 Guidance and manufacturer s declaration suussss 113 ixi exeroisciell necue cm 113 Emissions and immunity information YA LL LLAI LLL LC ALL LL FFF FF Fu 113 Advanced SEM cu Cnau y cis tq o n GG GA fS 117 General na ce Te Y Rd e CYFF oec dee den de s 117 Parameter S ran cio cn eat CNET CA aveo Tere Y atte cu eec ds 121 Data Management sy yne trn ld 125 NETWORK rettet ete Pete et Bd ut melee Edn YR 127 SGIVICQ e tote het ete ie
75. ed for accurate measurement Do not continuously measure beyond 10 minutes in any mode Ensure that probe covers are disposed of according to facility requirements or local regulations Return the probe to the probe well Wash your hands to reduce the risk of cross contamination Take a temperature in the Direct mode Direct mode displays the temperature of the probe as long as the probe tip remains in place at the measurement site and remains within the operating patient temperature range The patient s temperature will reach final equilibrium in approximately 3 minutes at the oral and rectal measurement sites and approximately 5 minutes at the axillary site The monitor enters Direct mode by the following methods e After you complete a Predictive mode measurement touch E to switch from Predictive to Direct mode The temperature frame in the lower eft corner changes to MODE Direct as it switches to the Direct mode e Remove the probe from the probe well load a probe cover select a temperature site and expose the probe to ambient air for more than 60 seconds to switch the monitor to Direct mode The temperature frame changes to MODE Direct e f you have a patient whose body temperature is below the normal temperature range and you follow the previous step the probe sensor identifies this condition and turns off the probe preheater in order to accommodate the lower body temperature measurement L WARNING Patient i
76. ended separation distance calculated Directions for use Guidance and manufacturer s declaration 115 Electromagnetic immunity from the eguation applicable to the freguency of the transmitter Recommended separation distance Conducted RF 3 Vrms 3 Vrms d 117 IP IEC 61000 4 6 150 kHz to 80 MHz Radiated RF 3V m 80 MHz to 1 GHz 3 V m de 1 17 A 80 to 800 MHz IEC 61000 4 3 P d 2 33 4 9o MHz to 2 5 GHz whereP is the maximum output power rating of the transmitter in watts W anddis the recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol t9 Note1 At 80 MHz and 800 MHz the higher frequency range applies Note 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which
77. ent The monitor enables you to take manual and automatic NIBP measurements A WARNING NIBP readings may be inaccurate for patients experiencing moderate to severe arrhythmia A WARNING Do not allow a blood pressure cuff to remain on neonatal patients more than 90 seconds when inflated above 5 mmHg Do not allow a blood pressure cuff to remain on the adult patients more than 3 minutes when inflated above 15 mmHg Excessive cuff tightness may cause venous congestion peripheral nerve injury discoloration of the limb and patient distress A WARNING Inaccurate measurement risk Pulse rate measurements generated through the blood pressure cuff or through SpO2 are subject to artifact and might not be as accurate as heart rate measurements generated through ECG or through manual palpation A WARNING Use caution when measuring blood pressure using oscillometric blood pressure devices in severely ill neonates and pre term infants because these devices tend to measure high in this patient population A CAUTION Inaccurate measurement risk Any external compression of the blood pressure hose or cuff may cause system errors or inaccurate measurements At the start of a measurement the monitor inflates the cuff to the appropriate level In the NIBP frame the systolic display shows the cuff inflation pressure while the blood pressure measurement is in progress The monitor measures blood pressure as the cuff is inflating If patient movement exc
78. ent Name Description Cancel button When touched the numeric keypad disappears and the selected number does not change OK button When touched the numeric keypad disappears and the entered number appears in the associated frame or data field Enter a number 1 With the numeric keypad open touch a number or numbers The value must be within the range that appears below the data field 2 Touch OK e f the value is within the required range and format the numeric keypad disappears and the entered numbers replace the previous numbers e fthe number is not within the required range and format OK remains inactive until you enter a valid number Close the numeric keypad Touch one of the following e OK Exits the numeric keypad and inserts the number e Cancel Exits the numeric keypad without saving entered numbers Open the keyboard Touch any field that includes the keyboard icon A The keyboard appears Keyboard patent 1D 01215908 tJ END d a Le JL Le o JE Le Le La LE Leis ESS a J 2J n 9 6 3 XT EB The keyboard includes the following components Directions for use Component 01215908 eger E Using the keypad keyboard and barcode scanner 43 Data field Backspace key Space bar Shift key Letters key Symbols key Diacritical marks key appearance varies in some languages Next button Cancel button O
79. er down the device High Network not found check network cable connections Low Powering down Call for service Low Battery is absent or faulty Call for service Low NIBP air leak check cuff and tubing connections Low NIBP not functional Call for service Low Unable to determine NIBP check connections and tubing for kinks Low Incorrect NIBP cuff size check patient type Low Inflation too quick check NIBP cuff and tubing connections Low Unable to determine NIBP check inflation settings Low 60 Alarms Welch Allyn Connex Vital Signs Monitor 6000 Series Alarm messages Priority Sp02 not functional Low Attach SpO2 sensor to monitor Low Replace the SpO2 sensor Low Set date and time Low Maximum number of patient records saved Oldest record overwritten Low Unable to access patient information Low Connect temperature probe Low Insert correct color coded probe well Low Replace temperature probe Low Temperature not functional Call for service Low Retry temperature measurement LOW Temperature time limit exceeded Retry temperature measurement Low Low battery plug into outlet Low Printer door is open close to continue Low Printer not functional Call for service Low Out of paper Low Printer too hot wait to retry Low Radio not functional Call for service Low Radio error Power down and restart Low Unable to establish network communications Radio out of network range Low Unable to establish netw
80. er that is not connected to the monitor and you have selected temperature as one of the four manual parameters to display Body Mass Index BMI is calculated and transferred to the monitor only by an attached weight scale You cannot enter or adjust BMI values BMI displays on the Manual tab and in the Manual parameters frame if you have selected it as one of the four parameters to display 40 Profiles Welch Allyn Connex Vital Signs Monitor 6000 Series Select a profile Follow these steps to select a profile which controls the appearance and functionality of the device 1 Touch Settings 2 Touch Profiles 3 Touch the desired profile 4 Touch Home to return to the Home tab Note Profiles cannot be changed while acquiring patient measurements or while unsaved patient measurements are on the display 41 Using the keypad keyboard and barcode scanner Open the numeric keypad Touch any field that includes the numeric keypad icon The numeric keypad appears Numeric keypad The numeric keypad includes the following components Component Name Description Data field Displays the numbers you enter The field name appears above and the range of values you can enter appears below this field ad Backspace key When touched removes the rightmost number from the data field 42 Using the keypad keyboard and barcode scanner Welch Allyn Connex Vital Signs Monitor 6000 Series Compon
81. ersion Select this to display primary units of measure and secondary units of measure for the temperature display on the Home tab Default SureTemp Plus site Select the default site for SureTemp measurements The default site applies when clinicians power up the monitor and each time clinicians remove the temperature probe from the well Directions for use Advanced settings 123 Select Last site to set the default to the site selected for the last measurement Do one of the following e _ To continue in the Advanced Settings touch another tab e _ To exit the Advanced Settings and return to the Home tab touch Exit Specify advanced SpO2 settings 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears Touch the Parameters tab Touch the SpO2 tab Specify settings Setting Action Description Default view Select a numeric view or a waveform view as the primary SpO2 display on the Home tab Default response Select the default speed of response to changes in SpO2 measurements Sweep speed Select the waveform sweep speed for the SpO2 display in the Home tab Do one of the following e _ To continue in the Advanced Settings touch another tab e To exit the Advanced tabs and return to the Home tab touch Exit Specify advanced SpHb settings i Access the Advanced Settings a Touch the Settings tab b
82. essage appears When multiple alarms occur the highest priority message appears You can cycle through each alarm message by touching the multiple alarm toggle Information messages instruct you to interact with the monitor in a specific way or provide information that does not require action You can dismiss an information message by selecting the control associated with the message or waiting for the message to time out Content area TEMPERATURE 98 3 F 36 89C PATIENT HEIGHT WEIGHT PAIN 13579 72 0 1971 3 The Content area displays vital sign measurements It also provides shortcuts to several controls The Content area includes the following frames e NIBP e SpO2 with optional SpHb e Pulse rate e Temperature e Patient e Manual parameters height weight pain temperature respiration and BMI depending on configuration 34 Navigation Welch Allyn Connex Vital Signs Monitor 6000 Series The Content area also includes a Save button which you use to manually save current measurements Save patient data Patient data can be saved to the monitor After taking a patient reading touch Save A message will appear indicating a successful or failed save Note You can configure some profiles and settings to automatically save measurements Navigation area The Navigation area includes the following tabs e Home Displays vital sign measurements and provides shortcuts to several controls e Patients
83. essive noise or an arrhythmia prevent the monitor from determining the blood pressure while the cuff is inflating the monitor attempts to measure the blood pressure while deflating the cuff When the measurement is complete the NIBP frame displays the measurement until you save it to the patient s record or you start another NIBP measurement Note The Pediatric and Adult blood pressure modes are supported on patients 29 days and older The Pediatric mode gives you the option of setting a lower initial inflation pressure when using the StepBP deflation and not SureBP 68 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series Note Use dual lumen tubes for adult and pediatric blood pressure measurements and single lumen tubes for neonate blood pressure measurements Mismatching tube types patient types and algorithms causes an information message to appear in the Device Status area For neonate patients set the NIBP settings as follows Patient Neonate Tube type 1 tube Algorithm Step Note Welch Allyn uses the following definition of Neonate Children 28 days or less of age if born at term 37 gestation or more otherwise up to 44 gestational weeks Take a manual NIBP measurement A WARNING Patient injury risk Never install Luer Lock connectors on Welch Allyn blood pressure cuff tubing Using these connectors on blood pressure cuff tubing creates the risk of mistakenly connecting this tubing to a patient s i
84. ette ho dec e E cie eade e tollent eue MUN tus 130 TEODORA M RH UAE 131 NIBFPrfessages cR ERROREM 131 SpO2 and SpHb messages sssssssssssssssseeeeeee eee 132 Temperature messages ci eae a dett 133 Weight scale messages sssssssssssssssssssee eee errem nennen nnnnis 134 Patient data management messages cece cece eceecceeeeceeeeeeceeeeeeeeeeeeeeeeeeeeeees 134 Radio messages ssssssssssessseeee em emere enne eene en LLY LL Ln nennen 135 Ethernet messages eee d etae ette oM ca P etel eatis 135 SNE A LM MU e A O 135 SyStermtressages suction eet te Dd tete eret esee deuten 136 Battery power manager messages sssssssssssssseeeeeeee eene 136 Configuration Manager messages ssssssssssss e eee 137 Printer messages ce E RE e ECT ER ERE 137 Problems and SOLIS ud Gen tte ie b RR 138 jYelerife p dicc 139 Approved aeceessori amp s ue rete eem eee eet set ER ee 139 Warranty eer t en NER RR RS fe one Sache wee ee a emet 146 vi Contents Welch Allyn Connex Vital Signs Monitor 6000 Series Introduction This manual describes the capabilities and operation of the monitor The information including the illustrations pertains to a monitor configured with noninvasive blood pressure NIBP body temperature pulse oximetry SpO2 total hemoglobin concentration SpHb pulse rate and weight scale options If your monitor configuration lacks any of these options some information in this manu
85. file which contains the Alarms tab 2 Touch the Alarms tab 3 Touch the NIBP tab 4 Enter the desired upper and lower alarm limits for systolic and diastolic measurements and MAP calculation using the up down arrow keys or the keypad 5 Touch the Home tab The new alarm settings display in the Alarm Limit control button Temperature Temperature frame From the temperature frame you can measure patient temperature Located in the lower right corner of the Home tab the temperature frame contains data and features relevant to temperature measurement The frame provides different features based on the profile you are using Temperature frame in Monitor profile TEMPERATURE 97 9 F 36 6 C Directions for use Patient monitoring 73 Temperature frame in Spot Check and Triage profiles TEMPERATURE 98 2 F 36 8 C Temperature measurement display In all profiles the frame can display temperature in Celsius or Fahrenheit You can configure the default view in Advanced settings Site selection Remove the temperature probe and touch the Temperature site control to toggle between sites Pediatric axillary Adult axillary Oral Note Monitors configured with the temperature module and the red rectal probe well and probe default to the rectal mode Rectal Note The monitor displays the ear mode when it receives a temperature measurement from the ear thermometer 74 Patient monitoring Welch A
86. gns Monitor 6000 Series Electromagnetic emissions Complies A WARNING This equipment system is intended for use by healthcare professionals only This equipment system may cause radio interference or may disrupt the operation of nearby equipment It may be necessary to take mitigation measures such as re orienting or relocating the monitor or shielding the location 8 The monitor contains a 5 GHz orthogonal frequency division multiplexing transmitter or a 2 4 GHz frequency hopping spread spectrum transmitter for the purpose of wireless communication The radio is operated according to the requirements of various agencies including FCC 47 CFR 15 247 and R amp TTE Directive 1995 5 EC The transmitter is excluded from the EMC requirements of 60601 1 2 but should be considered when addressing possible interference issues between this and other devices Electromagnetic immunity The monitor is intended for use in the electromagnetic environment specified below The customer or the user of the monitor should assure that it is used in such an environment Immunity test Electrostatic discharge ESD EC 61000 4 2 Electrical fast transient burst EC 61000 4 4 Surge IEC 61000 4 5 Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 IEC 60601 test level 6 kV contact x 8 kV air 2 kV for power supply lines 1 kV for input output lines 1 kV differen
87. gns Monitor 6000 Series Spot Check profile The Spot Check profile is optimized for clinicians who take spot check vitals readings and do not need automatic reading or alarm features i 8345097245 4A West OERA 12 31 2011 TEMPERATURE 98 0 9F 36 79C PATIENT HEIGHT WEIGHT PAIN 13579 720 1971 3 Triage profile The Triage profile allows for vital signs capture without alarms or access to the Patients tab 5 8345097245 4A West TEMPERATURE 98 1 F 36 79C PATIENT Directions for use Profiles 39 Profile feature comparison The following table compares the features of the profiles Feature Monitor Spot Check Triage Take NIBP SpO2 X X X temperature and pulse rate readings Take SpHb readings Masimo X only Configure and use interval X timing setting Observe and configure alarm X limits Observe and respond to X physiological alarms Change patient type adult X X X pediatric neonate View and enter manual X X parameters height weight pain respiration temperature BM Save currently displayed data X X X to device memory Save and review patient data X X X Access Patients tab X X Access Alarms tab X Access Review tab X X X Access Settings tab X X X Braun IR thermometers configured to work with the monitor transfer temperature data automatically to the Temperature frame You can enter temperature manually if you take a patient temperature with a thermomet
88. he patient and reapply The monitor may have the SpHb license but the Contact Welch Allyn to verify Sp02 module does not that the SpO2 module contains the SpHb license No weight measurement is The scale is not connected Inspect the USB cables from the transferred from the scale to the device to the adapter to the scale monitor to ensure that they are connected properly The scale setting is incorrect Ensure that the scale settings are enabled for transfer 139 Appendix Approved accessories The following tables list approved monitor accessories and documentation For information about options upgrades and licenses refer to the service manual FlexiPort cuffs Latex free Part Number Model Description Reuse 08 Reusable Cuff reuse SM CHILD 2 tube Reuse 09 Reusable Cuff reuse CHILD 2 tube Reuse 10 Reusable Cuff reuse SM AD 2 tube Reuse 11 Reusable Cuff reuse ADULT 2 tube Reuse 11L Reusable Cuff reuse AD LONG 2 tube Reuse 12 Reusable Cuff reuse LG AD 2 tube Reuse 12L Reusable Cuff reuse LG AD LONG 2 tube Reuse 13 Reusable Cuff reuse THIGH 2 tube Soft 08 Disposable Cuff soft SM CHILD 2 tube box of 20 Soft 09 Disposable Cuff soft CHILD 2 tube box of 20 Soft 10 Disposable Cuff soft SM AD 2 tube box of 20 Soft 11 Disposable Cuff soft ADULT 2 tube box of 20 Soft 11L Disposable Cuff soft AD LONG 2 tube box of 20 Soft 12 Disposable Cuff soft LG AD 2 tube box of
89. he Device Status area See note below Touch Continue to touch multiple alarm toggle buttons and to reset tones until you have read all of the messages Note The multiple alarm toggle button will display the number of active alarms inside the alarm icon A set of dots indicating the display order of alarms from highest left to lowest right priority as well as the most recent in the case of multiple alarms of the same priority will appear below it Directions for use Alarms 57 Adjust vital sign alarm limits You can adjust vital sign alarm limits or turn off alarm limit checking for individual parameters A A WARNING Alarm limits are user adjustable All alarm limit settings should take into account the patient s condition and acute care needs Appropriate alarm limits should be set accordingly for each patient CAUTION Loss of power will cause the monitor to return to default settings Each time you power up the monitor you must set alarm limits appropriate for your patient 1 On the Home tab touch the alarm limits control in the selected parameter frame For example to adjust the NIBP alarm limits touch 2 Adjust vital sign alarm limits e To adjust a limit Enter the desired upper and lower alarm limits using the up down arrow keys or the keypad e _ To turn alarm limits off or on for the vital sign Touch o or or This button toggles to display the current alarm state If you turn off alarm l
90. he SpO2 cable sssssssssssseee memes 24 Attach an accessory i vite d e e ee ta tte dte d 24 Detach an accessory cocoococooocnnonononcnnconnonononnnnnnn nro em enne nennen FFF EErEE EEE 25 Insert a new roll of paper iter eer GL Fy FFF cede Es 25 Connect AG DOWEL x eet repetere Uds mda e e e pede e TUR p tae dn 26 Disconnect AC DOWOFr sie teet fee recedit queso eda e E 26 SS LANDON ay mm 27 POWE en soar YD ey nce Neri bee ty temen Eris Badass ei elastin Ge TEA 27 Power Up the MONItOl sas as dts eter eter Ge ete ited 28 Power GOWN the mobltor ett RG tati 29 RESET THE MONITOR a rt re A ee A dE 29 Seite date anu UIE i n cett trem etd Pectora eo a ree 29 Enter cliniclan INFORMATION usi rere e p e Pe fe Pr ea e eH E Pepe nee 30 Set the defaulticonfigurdtlOn cumpa anta little ii 30 A a Yf Dd Gy Fo Od yn es A du WA 31 Fortiextabs A erstes htm Av us Acida 31 iv Contents Welch Allyn Connex Vital Signs Monitor 6000 Series Device Status drea s er ee ote A 31 CIMENTA G d entier A 33 Navigation area ce y y yy yn aere e ple Y Y Yy O 34 eiu ou M EYES E EE E EEE dri UM OUR uA o FT a Pres Ee PEDE E 37 Selecta pili het Nec bd iere o pec y el 40 Using the keypad keyboard and barcode scanner 41 Open the numeric ke Padua eeu oe ce te et D ette Dei 41 Numeric keypad tien KE iE 41 Enter an unben ote ed teet idee rtt det ette edet shel eet 42 Close the numere Keypad cepere eee 42 Open the
91. he default setting is the Predictive mode 76 Patient monitoring A A Welch Allyn Connex Vital Signs Monitor 6000 Series WARNING Inaccurate measurement risk To ensure optimal accuracy always confirm that the correct mode and site are selected WARNING Patient injury risk Do not exceed the recommended temperature measurement durations in Direct mode Continuous measurement durations of 3 minutes at the oral and rectal sites and 5 minutes at the axillary site are recommended for accurate measurement Do not continuously measure beyond 10 minutes in any mode Directions for use Patient monitoring 77 Predictive mode Is a one time measurement that takes a temperature in approximately 6 to 15 seconds Removing the probe from the probe well loading a probe cover and holding the probe tip in place at the measurement site initiates a Predictive mode measurement The monitor sounds a tone to indicate the end of a predictive measurement Direct mode Provides continual temperature measurements For oral and rectal measurements it is recommended to measure temperature until the temperature stabilizes or for 3 minutes For axillary measurements it is recommended to measure temperature until the temperature stabilizes or for 5 minutes The monitor changes to Direct mode approximately 60 seconds after the probe is removed from the probe well A CAUTION The monitor does not retain Direct mode temperatures in memory Therefore it is
92. he monitor to AC power immediately after inserting a new battery Mount the monitor on a stand 1 Align the monitor on the black plate in the center of the stand tray 2 Tighten the screw on the plate into the screw hole on the back of the monitor Mount the monitor on the wall For mounting instructions see the wall mount manufacturer s directions for use Attach the probe well 1 Align the probe well with the tabs facing up and down and insert the probe well into the temperature module Directions for use Setup 21 The probe well snaps into place when it is fully seated 2 Insert the temperature probe into the probe well Attach the temperature probe A CAUTION The temperature module only operates with the probe well properly in place 1 Remove the cover of the temperature module by pressing the tab and sliding the cover to the right The cover is located at the bottom right of the monitor below the probe well 2 Hold the temperature probe cable connector with the spring tab on the right and insert it into the probe port of the temperature module 22 Setup Welch Allyn Connex Vital Signs Monitor 6000 Series 3 Push it into place until it clicks 4 Reattach the cover Use the alignment tab and slide the cover to the left to click it back into place Remove the temperature probe and well Follow these steps to disconnect the probe cable and remove the probe well 1 Remove the cover of the tempe
93. ift the monitor by the power supply cord or patient connections Routinely inspect the AC power cord blood pressure cuff SpO2 cable and other accessories for strain relief wear fraying or other damage Replace as necessary WARNING Fire and explosion hazard Do not operate the monitor in the presence of a flammable anesthetic mixture with air oxygen or nitrous oxide in oxygen enriched environments or in any other potentially explosive environment WARNING Fire and shock hazard Only connect LAN cables contained within the perimeter of a single building Conductive LAN cables spanning multiple buildings may introduce fire or shock hazards unless they are fitted with fiber optic cables lightning arrestors or other applicable safety features Directions for use gt gt gt gt gt PDP P gt P bb About warnings and cautions 11 WARNING The monitor may not function properly if dropped or damaged Protect it from severe impact and shock Do not use the monitor if you notice any signs of damage Qualified service personnel must check any monitor that is dropped or damaged for proper operation before putting the monitor back into use WARNING Defective batteries can damage the monitor If the battery shows any signs of damage or cracking it must be replaced immediately and only with a battery approved by Welch Allyn WARNING Improper disposal of batteries may create an explosion or contamination hazard Never dispose of b
94. illary site are recommended for accurate measurement Do not continuously measure beyond 10 minutes in any mode A WARNING Probe covers are single use only Re use of a probe cover may result in spread of bacteria and cross contamination Directions for use A Patient monitoring 75 WARNING Patient injury risk Use only Welch Allyn single use disposable probe covers Never take a temperature measurement without a single use probe cover securely attached Failure to use a probe cover can cause patient discomfort from a heated probe patient cross contamination and inaccurate temperature readings WARNING Patient illness may result from improper use of oral and rectal temperature probes Using the incorrect probe may also produce inaccurate measurements e Use only oral probes identified by a blue ejection button at the top of the probe to take oral and axillary temperatures e Use only rectal probes identified by a red ejection button at the top of the probe to take rectal temperatures WARNING Patient illness or cross contamination may result from improper placement of oral and rectal temperature probes in the probe wells e Place only oral probes identified by a blue ejection button at the top of the probe in the blue probe wells e Place only rectal probes identified by a red ejection button at the top of the probe in the red probe wells WARNING Inaccurate measurement risk Never take an axillary temperature through
95. imit checking for a vital sign no visual or audio alarm signals will occur for those limits If alarm limit checking is off the icon changes to SS on the Home tab in the parameter frame Modify audio alarm notification You can modify the volume of all audio alarms Note A If the Allow user to turn off general audio option has been selected in Advanced settings you can turn off audio alarms but turning off alarms is not recommended in some circumstances such as unattended monitoring WARNING The alarm volume should be loud enough for you to hear it from where you are Set the volume considering the environment and ambient noise levels As you are working in the Alarms tab parameter measurements appear across the top of the tab 1 Touch the Alarms tab 58 Alarms Welch Allyn Connex Vital Signs Monitor 6000 Series TEMPERATURE 97 8 General NIBP Spo2 SpHb Pulse rate Temperature Limits Controls Volume Reset al ti ZO Cee QU Aam audio on High CL Hio Q Alarm audio off e Medium J Display alarm limits ee O Low 2 On the General tab modify audio alarm notification e To enable or disable audio alarms select Alarm audio on or Alarm audio off If you turn off audio alarms visual alarm signals still occur in the LED light bar Device Status area and on the Home tab in parameter frames The in the Device Status area indicates alarm audio turned off and a similar bell will appear in the pa
96. in V 19 5 H cm x 11 3 V cm 1024 H x 600 V 102 Specifications Welch Allyn Connex Vital Signs Monitor 6000 Series Protection classifications all monitor configurations Pixel arrangement RGB red green blue Color depth 16 bits per pixel Speaker volume Output sound pressure 67 dB at 1 0 meter Alarm and pulse tones per IEC 60601 1 8 Pulse frequency fp 150 1000 Hz umber of harmonic components in the minimum of 4 range 300 Hz to 4000 Hz Effective pulse duration ty high priority 75 200 ms medium and low priority 125 250 ms Rise time t 10 20 of ty Fall time t t t Note The relative sound pressure level of the harmonic components should be within 15 dB above or below the amplitude at the pulse frequency a Prevents overlap of pulses Battery specifications 6 cell 9 cell Rating 11 1 V 3 80Ah 42Wh 10 8 V 6 75Ah 73Wh Composition Lithium ion Lithium ion Charge time to 80 percent capacity 2hr 7m 2hr 25m Charge time to 100 percent capacity 3hr 4hr Patient exams per charge 26 47 Age to 70 percent capacity 300 300 1A patient exam includes NIBP Temperature and SpO2 measurements at the rate of one patient every 10 minutes with a 2 minute display time out setting and a new battery 2After this many full charge and discharge cycles the battery has aged to where its total capacity has been reduced to 70 percent of its rating Nurse Call connection specifications Nurse C
97. ing the Monitor profile which contains the Alarms tab Touch the Alarms tab Touch the SpHb tab Enter the desired upper and lower alarm limits for SpHb using the up down arrow keys or the keypad Touch the Home tab The new alarm settings appear in the Alarm Limit control button 92 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series Set SpHb averaging mode JW i Touch in the SpHb frame The SpHb frame displays the current mode Pulse rate frame The pulse rate frame located in the upper right of the Home tab displays data information and controls used in reading pulse rates Typically the displayed pulse rate is derived from the SpO2 sensor If SpO2 is not available the pulse rate is derived from NIBP A WARNING Inaccurate measurement risk Pulse rate measurements generated through the blood pressure cuff or through SpO2 are subject to artifact and might not be as accurate as heart rate measurements generated through ECG or through manual palpation Note You can specify pulse tone volume in the Pulse rate tab located in the Alarms tab Monitor profile Spot Check and Triage profiles Configure pulse rate alarms Follow these steps to set alarm limits for pulse rate Verify that you are using the Monitor profile which contains the Alarms tab Touch the Alarms tab Touch the Pulse rate tab ToO qum Enter the desired upper and lower alarm limits for pulse rate using the up down
98. isk Frequently inspect the probe window and keep it clean dry and undamaged Fingerprints cerumen dust and other contaminants reduce the transparency of the window and result in lower temperature measurements To protect the window always keep the thermometer in the accessory dock when the thermometer is not in use CAUTION Inaccurate measurement risk Before taking a temperature measurement make sure that the ear is free from obstructions and excess cerumen build up CAUTION Inaccurate measurement risk The following factors can affect ear temperature measurements for up to 20 minutes e The patient was lying on his or her ear e The patient s ear was covered e The patient was exposed to very hot or very cold temperatures e The patient was swimming or bathing e The patient was wearing a hearing aid or an ear plug Directions for use Patient monitoring 83 A CAUTION Inaccurate measurement risk If ear drops or other ear medications have been placed in one ear canal take the temperature in the untreated ear Note A temperature measurement taken in the right ear might differ from a measurement taken in the left ear Therefore always take the temperature in the same ear Note When the monitor receives an ear temperature measurement it displays the measurement on the Home tab If the Home tab already contains a temperature measurement the new measurement overwrites it To take a measurement and transfer it to the monitor
99. le such devices may be useful for verifying that the pulse oximeter sensor cabling and monitor are functional they are incapable of providing the data required to properly evaluate the accuracy of a system s Sp02 measurements Fully evaluating the accuracy of the Sp02 measurements requires at a minimum accommodating the wavelength characteristics of the sensor and reproducing the complex optical interaction of the sensor and the patient s tissue These capabilities are beyond the scope of known bench top testers Sp02 measurement accuracy can only be evaluated in vivo by comparing pulse oximeter readings with Sa02 measurements obtained from simultaneously sampled arterial blood made using a laboratory CO oximeter Many functional testers and patient simulators have been designed to interface with the pulse oximeter s expected calibration curves and may be suitable for use with Nellcor monitors and or sensors Not all such devices however are adapted for use with the Nellcor OXIMAX digital calibration system While this will not affect use of the simulator for verifying system functionality displayed SpO2 measurement values may differ from the setting of the test device For a properly functioning monitor this difference will be reproducible over time and from monitor to monitor within the performance specifications of the test device SpHb specifications refer to sensor manufacturer s directions for use for additional information SpHb sat
100. lem descriptions that do not generate messages to help you troubleshoot issues on the monitor Note Problem descriptions without messages appear at the end of this section When the monitor detects certain events a message appears in the Device Status area at the top of the screen Message types include the following e Information messages which appear on a blue background Very low priority alarms which appear on a cyan background e ow and medium priority alarms which appear on an amber background e High priority alarms which appear on a red background Technical alarm messages are low or very low priority unless noted in the Message column You can dismiss a message by touching the message on the screen or for some messages you can wait for the message to time out To use these tables locate the message that displays on the monitor in the left column of the table The remainder of the row explains possible causes and suggests actions that can resolve the issue Note Instructions to Call for service in the following tables mean that you should contact qualified service personnel in your facility to investigate the issue NIBP messages Message Possible cause Suggested action NIBP air leak check cuff and tubing The NIBP module has an air leak Check the cuff and tubing connections connections Clear the alarm and retry NIBP NIBP not functional Call for A module error occurred Call for service service U
101. llyn Connex Vital Signs Monitor 6000 Series Temperature buttons The buttons on the right side of the frame enable you to do different tasks depending on the profile you are using The availability of functions depends on which profile is selected Button name Button image Description This button displays alarm limits and status Touch the button to display the Alarms tab Temperature alarm Direct mode ry Touch the button to enter Direct mode Configure temperature alarms Follow these steps to set alarm limits for temperature measurement Verify that you are using the Monitor profile which contains the Alarms tab Touch the Alarms tab Touch the Temperature tab a m Enter the desired upper and lower alarm limits for temperature using the up down arrow keys or the keypad 5 Touch the Home tab The new alarm settings display in the Alarm Limit control button SureTemp Plus temperature module The temperature module uses a thermistor thermometer design and a predictive algorithm to calculate patient temperatures in the Predictive mode N WARNING Patient injury risk Prior to taking a temperature instruct the patient not to bite down on the probe as patient injury and damage to the probe may result A WARNING Patient injury risk Do not exceed the recommended temperature measurement durations in Direct mode Continuous measurement durations of 3 minutes at the oral and rectal sites and 5 minutes at the ax
102. mation about thermometer functionality refer to the thermometer manufacturer s directions for use Change the temperature scale on the ear thermometer To switch from Celsius to Fahrenheit refer to the thermometer manufacturer s directions for use Charge the ear thermometer battery To charge the battery pack e Place the thermometer in the accessory dock 84 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series e Make sure that the monitor is connected to AC power e Make sure that the monitor is powered on The LED on the dock indicates the charging status of the battery pack e Orange The battery pack is charging e Green The battery pack is charged e Not illuminated The battery pack is not charging Note The battery pack continues to charge while the monitor is in Display power saving mode Note It is strongly recommended that you use only the Welch Allyn rechargeable battery pack in the thermometer because the dock cannot charge other batteries Sp02 SpO2 and pulse rate monitoring continuously measures saturation level of oxygen in hemoglobin as well as the pulse rate in a patient through a pulse oximeter Sp02 frame The SpO2 frame displays data and controls used in pulse oximetry measurements The frame provides a numeric view and a waveform view of SpO2 data You can toggle between views by touching the left side of the frame SpO2 numeric view The numeric view indicates the SpO2 saturati
103. mmable anesthetics e near electro cauterization devices For contraindications of SpO2 and SpHb sensors consult the sensor manufacturer s directions for use Symbols Documentation symbols A N A Lli Power symbols Al GQ A WARNING The warning statements in this manual identify conditions or practices that could lead to illness injury or death Caution The caution statements in this manual identify conditions or practices that could result in damage to the equipment or other property or loss of data This definition applies to both yellow and black and white symbols WARNING Hot surface Do not touch Consult operating instructions Power on standby on the display monitor is plugged into Alternating Current Cx power on the monitor green indicator Alternating Current power present battery fully charged on the monitor amber indicator Alternating Current power C present battery is charging Alternating Current AC a AS Equipotential terminal Battery absent or faulty Battery charge level Battery cover Rechargeable battery 4 Symbols Gon Li ion battery Connectivity symbols lt all USB Wireless signal strength Best 4 bars Good 3 bars Fair 2 bars Weak 1 bar No signal no bars No connection blank Miscellaneous symbols C 0297 usd D t D Meets essential requirements of European Medical Device Directive 93
104. n place at the oral or rectal measurement site for a total of 3 minutes and for 5 minutes at the axillary site 5 While the measurements are taking place the temperature frame displays the patient s continuous temperature measurements in degrees Fahrenheit and degrees Celsius TEMPERATURE 97 9 F 36 6 C Note The monitor does not retain Direct mode temperatures in memory Therefore it is important to note the temperature before removing the probe from the measurement site and then manually record it in the patient record 6 Remove the probe after the temperature measurement is complete and firmly press the eject button on the top of the probe to release the probe cover 7 Return the probe to the probe well to continue taking temperatures in the Predictive mode 8 Wash your hands to reduce the risk of cross contamination Take a temperature at the rectal site A WARNING Patient injury risk When taking rectal temperatures insert the probe tip only 5 8 inch approximately 1 5 cm inside the rectum of adults and only 3 8 inch approximately 1 cm inside the rectum of children to avoid the risk of bowel perforation A WARNING Cross contamination or nosocomial infection risk Thorough hand washing greatly reduces the risk of cross contamination and nosocomial infection A WARNING Patient injury risk Do not exceed the recommended temperature measurement durations in Direct mode Continuous measurement durations of 3 mi
105. n to the Home tab touch Exit Set and start the demo mode 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the General tab 3 Touch the Demo tab 4 Specify settings Setting Action Description Type Select a type of demonstration mode Start Touch Start to put the monitor in demonstration mode Navigate to the Home tab to begin Demo mode 5 Do one of the following e _ To continue in the Advanced Settings touch another tab e Toexit the Demo mode touch Exit on the Home tab The monitor restarts automatically Parameters Specify advanced NIBP settings 1 2 4 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears Touch the Parameters tab Touch the NIBP tab Specify settings Setting Action Description Default view Select primary and secondary views Select Display MAP to display mean arterial pressure MAP in the NIBP frame on the Home tab 122 Advanced settings Welch Allyn Connex Vital Signs Monitor 6000 Series If Display MAP is selected specify which numerics are primary in the NIBP frame On the Home tab clinicians can touch the NIBP frame to toggle between views Default patient type Select a default patient type for this monitor The patient type shows in
106. nable to determine NIBP check The NIBP module experienced a motion artifact Check connections limit patient connections limit patient movement movement Clear the alarm and retry NIBP 132 Troubleshooting Welch Allyn Connex Vital Signs Monitor 6000 Series Message Possible cause Suggested action Unable to determine NIBP check The NIBP tubing has a kink Check the connections and tubing connections and tubing for kinks Clear the alarm and retry NIBP Incorrect NIBP cuff size check The cuff size is not correct Check the patient type patient type Clear the alarm and retry NIBP Inflation too quick check NIBP cuff NIBP inflation was too quick Check the connections and tubing and tubing connections for kinks Clear the alarm and retry NIBP Unable to determine NIBP check NIBP check inflation settings message Check inflation settings and inflation settings change as necessary Clear the alarm and retry NIBP Change the cuff inflation target CIT Excessive patient movement NIBP measurements are not accurate because of Limit patient movement during artifact blood pressure measurement Tube type does not match device The tube connected to the NIBP sensor does not Use the tube specified for the configuration match the monitor s configuration monitor NIBP measurement is available Tube type does not match device User is using a single lumen tube with the Clear message Modify settings configuration
107. nfigure use troubleshoot or maintain the thermometer A A A A WARNING Liquids can damage electronics inside the thermometer Prevent liquids from spilling on the thermometer If liquids are spilled on the thermometer dry off the thermometer with a clean cloth Check for proper operation and accuracy If liquids possibly entered the thermometer remove the thermometer from use until it has been properly dried inspected and tested by qualified service personnel CAUTION Probe covers are disposable nonsterilized and single use The thermometer is also nonsterilized Do not autoclave the thermometer and probe covers Ensure that probe covers are disposed of according to facility requirements or local regulations CAUTION The thermometer has no user serviceable parts If service is required call your nearest Welch Allyn Customer Service or Technical Support facility CAUTION Store the thermometer and probe covers in a dry location free from dust and contamination and away from direct sunlight Keep the ambient temperature at the storage location fairly constant and within the range of 50 F to 104 F 10 C to 40 C Take a temperature at the ear site A A A gt WARNING Probe covers are single use only Re use of a probe cover may result in spread of bacteria and cross contamination WARNING Inaccurate measurement risk Use only Braun ThermoScan probe covers with this thermometer WARNING Inaccurate measurement r
108. njury risk Do not exceed the recommended temperature measurement durations in Direct mode Continuous measurement durations of 3 minutes at the oral and rectal sites and 5 minutes at the axillary site are recommended for accurate measurement Do not continuously measure beyond 10 minutes in any mode WARNING Inaccurate measurement risk To ensure optimal accuracy always confirm that the correct mode and site are selected WARNING Patient injury risk Prior to taking a temperature instruct the patient not to bite down on the probe as patient injury and damage to the probe may result D D A CAUTION Probe covers are disposable nonsterilized and single use Probes are also nonsterilized Do not autoclave probes and probe covers Ensure that probe covers are disposed of according to facility requirements or local regulations 1 Remove the temperature probe from the probe well The monitor sounds a tone as it enters the ready state 2 Insert the probe into a new probe cover and press the probe handle down firmly 80 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series 3 Touch the Temperature site control Fed to choose from these measurement sites oral pediatric axillary or adult axillary The temperature frame changes to Direct mode approximately 60 seconds after the probe is removed from the probe well The monitor sounds a tone to indicate the start of a Direct mode measurement 4 Hold the probe tip i
109. nnex Vital Signs Monitor 6000 Series Welch Allyn jiddikjara li dan RLAN device jikkonforma mal htigijiet essenzjali u ma prowedimenti ohrajn relevanti li hemm fid Dirrettiva 1999 5 EC Welch AI disposic Welch Al yn declara que este RLAN device est conforme com os requisitos essenciais e outras es da Directiva 1999 5 CE yn t mto vyhlasuje ze RLAN device sp ia z kladn po iadavky a v etky pr slu n ustanovenia Smernice 1999 5 ES Siuo Wel Direktyvo ch Allyn deklaruoja kad Sis RLAN device atitinka esminius reikalavimus ir kitas 1999 5 EB s nuostatas Por medio de la presente Welch Allyn declara que el RLAN device cumple con los requisitos esenciales y cualesquiera otras disposiciones aplicables o exigibles de la Directiva 1999 5 CE H rmed intygar Welch Allyn att denna RLAN device st r verensst mmelse med de v sentliga egenskapskrav och vriga relevanta best mmelser som framg r av direktiv 1999 5 EG 113 Guidance and manufacturer s declaration EMC compliance Special precautions concerning electromagnetic compatibility EMC must be taken for all medical electrical eguipment This device complies with IEC EN 60601 1 2 2007 All medical electrical eguipment must be installed and put into service in accordance with the EMC information provided in this document and the Welch Allyn Connex Vital Signs Monitor 6000 Series Directions for Use Portable and mobile RF communications eguipme
110. nt can affect the behavior of medical electrical eguipment The monitor complies with all applicable and reguired standards for electromagnetic interference It does not normally affect nearby equipment and devices It is not normally affected by nearby equipment and devices It is not safe to operate the monitor in the presence of high frequency surgical equipment However it is good practice to avoid using the monitor in extremely close proximity to other equipment Emissions and immunity information Electromagnetic emissions The monitor is intended for use in the electromagnetic environment specified below The customer or user of the monitor should assure that it is used in such an environment Emissions test Compliance Electromagnetic environment guidance RF emissions Group 1 The monitor uses RF energy only for its internal function Therefore its CISPR 11 RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions Class A The monitor is suitable for use in all establishments other than CISPR 11 domestic establishments and those directly connected to the public Harmonic emissions Class A low voltage power supply network that supplies buildings used for domestic purposes provided the following warning is heeded IEC 61000 3 2 Voltage fluctuations flicker emissions IEC 61000 3 3 114 Guidance and manufacturer s declaration Welch Allyn Connex Vital Si
111. ntravenous line and introducing air into the patient s circulatory system A CAUTION Inaccurate measurement risk Any external compression of the blood pressure hose or cuff may cause system errors or inaccurate measurements 1 Properly size the blood pressure cuff and position it around the patient s bare upper arm 2 Touch Start to take a measurement Interval NIBP measurement The monitor can take NIBP measurements automatically based on intervals you choose The Intervals tab provides all interval features From this tab you can do the following e Configure intervals e Turn off intervals e Configure the monitor to print automatic measurements as they are completed When the measurement is complete the NIBP frame displays the measurement until the next measurement is complete Note During intervals each automatic and manual save of patient measurements clears all measurements from Manual parameters frame delis The E changes to a timer automatic measurement which counts down to the next Automatic measurements continue until you turn off intervals A WARNING Patient harm risk Do not use intervals on neonates out of earshot Verify that audio can be heard from where you intend to be Automatic print on interval The printer can be set to automatically print patient data at each interval Directions for use Patient monitoring 69 1 Touch the Settings tab 2 Touch the Intervals tab 3 Touch the b
112. nutes at the oral and rectal sites and 5 minutes at the axillary site are recommended for accurate measurement Do not continuously measure beyond 10 minutes in any mode WARNING Inaccurate measurement risk To ensure optimal accuracy always confirm that the correct mode and site are selected CAUTION Probe covers are disposable nonsterilized and single use Probes are also nonsterilized Do not autoclave probes and probe covers Ensure that probe covers are disposed of according to facility requirements or local regulations gt p gt Directions for use Patient monitoring 81 Remove the rectal temperature probe from the rectal probe well The monitor sounds a tone as it enters the ready state The Temperature Site Control defaults to the rectal site Insert the rectal probe into a new probe cover and press the probe handle down firmly Separate the patient s buttocks with one hand Use the other hand to gently insert the probe tip only 5 8 inch 1 5 cm inside the rectum of adults and only 3 8 inch approximately 1 cm inside the rectum of children The use of a lubricant is optional Insert the probe so that the tip is in contact with tissue Continue to separate the buttocks and hold the probe in place throughout the measurement process While the measurement is taking place the temperature frame displays the process indicator Va A The monitor sounds a tone when the final temperature is reached in approximately 10 to
113. on percentage and the pulse amplitude Features of this view differ based on the type of sensor enabled and the profile selected Nellcor sensor Monitor profile Spot Check and Triage profiles Masimo sensor Monitor profile Spot Check and Triage profiles Directions for use Patient monitoring 85 Pulse amplitude The pulse amplitude bar indicates the pulse beat and shows the relative pulse strength More bars illuminate as the detected pulse gets stronger Response Mode Control The Response Mode Control allows you to set the SpO2 measurement time to either Normal or Fast Perfusion index Perfusion Index Pl is an SpO2 feature available only with Masimo equipped monitors Pl is a relative reading of pulse strength at the monitoring site Pl is a numerical value that indicates the strength of the IR infrared signal returning from the monitoring site PI display ranges from 02 percent very weak pulse strength to 20 percent very strong pulse strength Pl is a relative number and varies between monitoring sites and from patient to patient as physiological conditions vary During sensor placement the Pl can be used to evaluate the appropriateness of an application site looking for the site with the highest PI number Placing the sensor at the site with the strongest pulse amplitude highest Pl number improves performance during motion Monitor the trend of the PI for changes in physiological conditions SatSecon
114. ons Welch Allyn Connex Vital Signs Monitor 6000 Series NIBP view 2 NIBP ce displays the MAP calculation as the primary content and the SYS DIA as secondary content The buttons on the right side of the frame enable you to do different tasks depending on the profile you are using The availability of functions depends on which profile is selected See the Profiles section for more information Button name Start Stop Interval Alarm Limit control Button image Description The appearance and function of this button dynamically changes Touch to start a manual measurement or a cycle of automatic measurements Touch to stop a measurement that is in progress This button shows the status of automatic measurements Touch the button to display the Intervals tab where you can configure automatic measurements prm Automatic measurements are off Automatic measurements are on This button displays alarm limits and status Touch the button to display the Alarms tab Select a cuff A WARNING Use only blood pressure cuffs and hoses listed as approved accessories to ensure safe and accurate NIBP measurements Directions for use A A Patient monitoring 65 WARNING Never use an adult or pediatric monitor setting or cuff for an NIBP measurement on a neonatal patient Adult and pediatric inflation limits can be excessive for neonatal patients even if a neonatal cuff is used Neonates are defined in the
115. or presents physiological alarms and technical alarms Physiological alarms occur when vital sign measurements fall outside of set alarm limits but they occur only in the Monitor profile Technical alarms occur in all profiles Note The three modes of data communication USB Ethernet and IEEE 802 11 are not intended for real time alarms Alarm types Type Priority Color Alarm audio tone e NIBP SpO2 or SpHb limit exceeded High Red 10 pulse tone e Some technical alarms Pulse rate limit exceeded Medium Amber 3 pulse tone e Some technical alarms Temperature limit exceeded Low Amber 2 pulse tone or 1 pulse tone e Some technical alarms Alarm notification locations A WARNING If you are relying on visual alarm notifications maintain a clear line of sight with the monitor and or Nurse Call If you are relying on audio alarm notifications ensure that you can hear audio alarms from where you are Set the volume as needed considering the environment and ambient noise levels Nurse Call When the Nurse Call cable is connected and Nurse Call has been enabled the monitor immediately notifies the Nurse Call system when an alarm occurs Nurse Call notification settings are specified in the Advanced settings LED light bar The light bar on the handle of the monitor illuminates as follows e Flashing red for high priority alarms 54 Alarms Welch Allyn Connex Vital Signs Monitor 6000 Series e Flashing amber for medium priority
116. ork communications Call for Service Low Unable to establish network communications Call for Service Low Radio software upgrade failed Low Unable to load configuration using factory defaults Low Functional error Call for service Low External device not recognized Low Incompatible Welch Allyn device Low Directions for use Alarms 61 Alarm messages Priority USB Communication failure Low Low battery 30 minutes or less remaining Low Low SpHb signal quality Check sensor Low Low Sp02 signal quality Check sensor Low Low perfusion Check sensor Low Replace the SpO2 cable Low Sp02 mode only Check sensor or cable Low Sp02 sensor expires in Low Unexpected restart occurred Call for service Low Weight scale not functional Call for service Low Nurse call The monitor can be connected to a Nurse Call system through a cable that connects to the Nurse Call connector When the Nurse Call cable is connected and Nurse Call is enabled the monitor immediately notifies the Nurse Call system when a physiological alarm that exceeds the preset threshold occurs The Nurse Call system is also synchronized with the flashing LED lightbar and audible alerts on the monitor Nurse Call thresholds are set in the Advanced Settings To connect the monitor to a Nurse Call system you must have a cable that has been adapted to your Nurse Call system REF 6000 NC rated 25V AC or 60V DC maximum at 1A maximum For ordering information
117. ouch Next This control accepts the entry for the current field then clears the data field to allow data entry in the next field e Touch OK The keyboard disappears and the entered characters appear in the data field Enter a symbol or special character Note To return to the keyboard s normal layout touch ABC 1 With the keyboard open touch 216 Symbols and special characters for the selected language appear aio ea 2 Touch the appropriate symbol or special character The keyboard returns to its normal layout Enter a diacritical mark Note Keyboards with diacritical marks are available only for languages that use diacritical marks Note To return to the keyboard s normal layout without saving changes touch Diacritical marks key Language s None Not applicable Danish English Dutch German Italian 13 French Ya Finnish Norwegian Spanish Swedish e 3i Portuguese Directions for use Using the keypad keyboard and barcode scanner 45 Diacritical marks key Language s mem Polish Greek AE With the keyboard open touch the diacritical marks key This key varies based on the language as noted above The keyboard displays diacritical marks for the selected language and therefore varies from one language to another On each diacritical marks keyboard the letters key in the top left corner returns you to the standard keyboard Touch a diacritical mark The keyboard returns
118. ox next to Automatic print on interval Automatic intervals You can configure the monitor to take automatic NIBP measurements at consistent intervals Intervals Device Clinician Profiles Advanced e Automatic Minutes Program 15 MM Qs c 1 240 Automatic print on interval Start intervals Settings pu Note An alarm does not turn off intervals Subsequent automatic measurements continue to occur as scheduled Start automatic intervals Follow these steps to configure the monitor to take NIBP measurements at consistent intervals 1 Properly size the blood pressure cuff and position it around the patient s bare upper arm On the Home tab touch Select Automatic Use the numeric keypad to enter the length of time between NIBP measurements Or e Qu 9 Touch Start intervals Note Intervals are not available in all profiles See the Profiles section for more information Program intervals You can configure the monitor to take automatic NIBP measurements at variable intervals The monitor comes with preset interval programs that can be edited to meet your needs The numbers below the program name indicate the length of time between each interval in the cycle 70 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series Intervals Device Clinician Profiles Advanced EN Ln rr e Duration Interval amp Program gram 2 5 BH o Q Stat Program 2 go go Automatic
119. plays MODE Fast when Fast mode is selected Directions for use Patient monitoring 89 SpHb Monitors configured with Masimo total hemoglobin can measure hemoglobin SpHb SpO2 and pulse rate SpHb monitoring continuously measures blood constituents and anemic status in a patient through a noninvasive SpHb pulse co oximeter SpHb frame The SpHb frame displays data and controls used in total hemoglobin measurements Note SpHb is available only in the Monitor profile In this frame one of two labels appears e SpHbv indicates the venous calibrated reference for total hemoglobin measurement e _ SpHb indicates the arterial calibrated reference for total hemoglobin measurement You can specify the reference source in Advanced settings The frame provides a numeric view and a graphical trend view of total hemoglobin data You can toggle between views by touching the left side of the frame SpHb numeric view The numeric view indicates the total hemoglobin level in either grams per deciliter g dL or millimoles per liter mmol L You can select the unit of measure in Advanced settings Averaging The averaging button enables you to select the moving window of time used by the parameter to calculate the SpHb value and update the display short approximately 1 minute medium approximately 3 minutes or long approximately 6 minutes Y ov Y NA SpHb graphical trend view The graphical trend view presents a trend of the re
120. power outlet and the battery is charging or is fully charged The estimated charge rate is displayed as a percentage of capacity e The monitor is not connected to a power outlet and is running on battery power The estimated charge time remaining is displayed in the hour s minute s format Each section of the battery status indicator represents a percentage of remaining charge e The monitor is connected to a power outlet but the battery does not maintain a charge or has been removed wd IN When the battery is not being recharged and power becomes low a low priority alarm appears in the Device Status area Directions for use Navigation 33 Note Observe the remaining battery charge in the battery status indicator and plug the monitor into a power outlet as soon as you are able If the low priority alarm is dismissed or if you take no action to charge the battery a high priority alarm appears when battery power is critically low Plug the monitor into a power outlet immediately to prevent it from shutting down A Low battery 5 minutes or less remaining Alarm and information messages The Device Status area provides alarm and information messages that are either temporary or exist as long as the condition to which the message applies remains Alarm or information messages may also include controls and or behavior that you can use to manage alarm and information messages When the monitor detects an alarm condition an alarm m
121. rameter frames If an alarm condition occurs the bell will be red or amber in the alarming frame according to the priority of the alarm as shown here e To modify the volume of audio alarms Select a volume level An audio tone sounds briefly to indicate the volume level Note Periodically test the speaker by selecting different speaker volumes and listening for the different tones Alarm messages and priorities The following tables list the physiological and technical alarm messages and their priority Physiological alarms Alarm messages Priority Alarm limit exceeded NIBP systolic HIGH High Alarm limit exceeded NIBP systolic LOW High Directions for use Alarms 59 Alarm messages Priority Alarm limit exceeded NIBP diastolic HIGH High Alarm limit exceeded NIBP diastolic LOW High Alarm limit exceeded NIBP MAP HIGH High Alarm limit exceeded NIBP MAP LOW High Alarm limit exceeded Pulse rate HIGH edium Alarm limit exceeded Pulse rate LOW Medium Alarm limit exceeded SpO2 HIGH High Alarm limit exceeded Sp02 LOW High Alarm limit exceeded SpHb HIGH High Alarm limit exceeded SpHb LOW High Alarm limit exceeded Temperature HIGH Low Alarm limit exceeded Temperature LOW Low Technical alarms Alarm messages Priority Low battery 5 minutes or less remaining High Searching for pulse signal High Communications module did not power on properly Pow
122. rature module by pressing the tab and sliding the cover to the right The cover is located at the bottom right of the monitor below the probe well 2 Depress the spring tab on the temperature probe cable connector and withdraw it from the probe port 3 Reattach the cover Use the alignment tab and slide the cover to the left to click it back into place Grasp the probe well and pull it up to remove it from the monitor Connect the NIBP hose 1 Place your thumb and forefinger on the hose connector and squeeze the side tabs 2 Align the hose connector with the hose connector port on the side of the monitor Directions for use Setup 23 3 Insert the hose connector pressing firmly until it clicks into place Disconnect the NIBP hose 1 Place your thumb and forefinger on the hose connector Note Always grasp the hose by the connector Do not pull on the hose itself 2 Squeeze the side tabs until the connector releases 3 Pull the connector away from the connector port Connect the SpO2 cable A WARNING Patient injury risk Do not use a damaged sensor or pulse oximetry cable or a sensor with exposed electrical or optical components 1 Place your thumb and forefinger on the SpO2 cable connector and squeeze the side tabs 2 Align the cable connector with cable connector port 3 Insert the cable connector pressing firmly until it clicks into place 24 Setup Welch Allyn Connex Vital Signs Monitor 6000 Series
123. rections for use Clear clinician information on manual save Advanced settings 127 Clinician tab Returned clinician information populates the Device Status area and fields on the Clinician tab Selec enter tab Th Require password to require clinicians to their password in addition to ID on the Clinician e monitor uses the ID and password combination to query the network for clinician information Speci y that the monitor clears the selected clinician after a clinician manually saves measurements from the Home tab Clinician information clears from the Clinician tab and the Device Status area 5 Doone ofthe following To continue in the Advanced Settings touch another tab To exit the Advanced Settings and return to the Home tab touch Exit Specify clinical data settings 1 Access the Advanced Settings a b C d Touch the Settings tab Touch the Advanced tab Enter the Advanced settings code Touch OK The General tab appears Touch the Data Management tab Touch the Clinical Data tab 4 Specify settings Setting Automatically send on manual save Se to the network when a clinician saves measurements on the Home tab Delete readings after successful send Se de ect ect Action Description his option to specify that measurements are sent his option to specify that measurements are eted from the monitor after they are successfully sent to the netwo
124. rektiivist tulenevatele teistele asjakohastele s tetele Welch Allyn vakuuttaa t ten ett RLAN device tyyppinen laite on direktiivin 1999 5 EY oleellisten vaatimusten ja sit koskevien direktiivin muiden ehtojen mukainen Par la pr sente Welch Allyn d clare que ce RLAN device est conforme aux exigences essentielles et aux autres dispositions de la directive 1999 5 CE qui lui sont applicables Hiermit erkl rt Welch Allyn die bereinstimmung des Ger tes RLAN device mit den grundlegenden Anforderungen und den anderen relevanten Festlegungen der Richtlinie 1999 5 EG Wien ME THN IIAPOYZA Welch Allyn AHAONEI OTI RLAN device SYMMOP QNETAI IIPOX TIX OY2IOAEI AIIAITHXEI gt KAI TIX AOIIIEX XXETIKEX AIATAZEIX THX OAHTTAX 1999 5 EK Alul rott Welch Allyn nyilatkozom hogy a RLAN device megfelel a vonatkoz alapvet k vetelm nyeknek s az 1999 5 EC ir nyelv egy b el r sainak Con la presente Welch Allyn dichiara che questo RLAN device conforme ai requisiti essenziali ed alle altre disposizioni pertinenti stabilite dalla direttiva 1999 5 CE Ar o Welch Allyn deklar ka RLAN device atbilst Direkt vas 1999 5 EK b tiskaj m pras b m un citiem ar to saistitajiem noteikumiem Siuo Welch Allyn deklaruoja kad Sis RLAN device atitinka esminius reikalavimus ir kitas 1999 5 EB Direktyvos nuostatas 112 Standards and compliance Malti Portuguese Slovak Slovene Spanish Swedish Hawnhek Welch Allyn Co
125. remains in place Prolonged impairment of circulation or improper cuff position can cause bruising Current cuff pressures are not dynamically displayed during a Stat reading The Home tab displays the NIBP reading from the previous cycle until the current cycle finishes STOP Note If you are in Stat intervals you can stop intervals by touching If you touch the button twice you will restart Stat intervals The control toggles between STOP and START with each touch Start Stat intervals Follow these steps to start Stat intervals 1 Properly size the blood pressure cuff and position it around the patient s bare upper arm 2 Select Stat Touch Start intervals Stop automatic measurements Follow these steps to turn off intervals 1 On the Home tab touch the interval timer button 2 Touch Stop intervals Cancel a measurement that is in progress Follow these steps to cancel any NIBP measurement that is in progress 72 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series STOP On the Home tab touch The monitor rapidly deflates the cuff and the screen displays the NIBP cancellation message r5 01420 If intervals are turned on the button changes to a timer sil which counts down to the next automatic measurement Configure NIBP alarms Follow these steps to set alarm limits for systolic and diastolic measurements and MAP calculation 1 Verify that you are using the Monitor pro
126. rk Sent measurements do not appear in the Review tab Emulate Spot Vital Signs LXi Se network appears as Spot Vital Signs LXi data at the network 5 Doone ofthe following Network ect his option to specify that clinical data sent to the To continue in Advanced Settings touch another tab To exit the Advanced Settings and return to the Home tab touch Exit View advanced monitor information The Status tab shows the monitor s software version MAC and IP addresses network server and access point information session information and more 1 Access the Advanced Settings 128 Advanced settings Gu co om a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears Touch the Network tab Touch the Status tab View the information Do one of the following Welch Allyn Connex Vital Signs Monitor 6000 Series e _ To continue in the Advanced Settings touch another tab e To exit the Advanced Settings and return to the Home tab touch Exit Specify radio settings This task is applicable only to monitors that have a radio installed 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears Touch the Network tab Touch the Radio tab Specify settings Setting Enable radio Enable radio network alarm
127. ronment e moisture in the sensor e excessive ambient light especially fluorescent e the use of the wrong sensor e _ a sensor applied too tightly 1 Verify that the sensor cable is connected to the monitor A WARNING Patient injury risk The sensor and extension cable are intended only for connection to pulse co oximetry equipment Do not attempt to connect these cables to a PC or any similar device Always follow the sensor manufacturer s directions for care and use of the sensor 2 Clean the application site Remove anything such as nail polish that could interfere with sensor operation Note Do not use disposable sensors on patients who have allergic reactions to the adhesive 3 Attach the sensor to the patient according to the manufacturer s directions for use observing all warnings and cautions Note If a sterile sensor is required select a sensor that has been validated for sterilization and follow the sensor manufacturer s directions for sterilizing the sensor Place the sensor and the NIBP cuff on different limbs to reduce unnecessary alarms when you monitor these parameters at the same time 88 Patient monitoring Welch Allyn Connex Vital Signs Monitor 6000 Series Note A range of sensors is available for different patient sizes and measurement sites Consult the sensor manufacturer s instructions for selecting the correct sensor 4 Confirm that the monitor displays SpO2 and pulse rate data within 15 second
128. ropean Economic Community Waste Electrical and Electronic Eguipment Directive 2006 66 EC European Economic Community Batteries and Accumulators Directive SOR 98 282 Canadian Medical Devices Regulation IATA DGR International Air Transport Association Dangerous Goods Regulation United Nations ST SG AC 10 11 Manual of Tests and Criteria Part lll Sub Section 38 3 ANSI AAMI SP10 AS NZS 3200 1 0 ASTM D 4332 E 1104 CAN CSA C22 2 NO 601 1 CAN CSA C22 2 NO 60601 1 2 CSA Z9919 EN 1060 1 1060 3 1060 4 EN IEC 60601 1 60601 1 2 60601 1 4 60601 1 6 60601 1 8 60601 2 30 60601 2 49 62304 EN ISO 9919 13485 14971 ISTA 2A UL 60601 11 K Directive 2002 96 EC WEEE Disposal of noncontaminated electrical and electronic equipment This product and its accessories must be disposed of according to local laws and regulations Do not dispose of this product as unsorted municipal waste Prepare this product for reuse or separate collection as specified by Directive 2002 96 EC of the European Parliament and the Council of the European Union on Waste Electronic and 1 Standard is essentially the IEC 60601 1 General standard plus the listed country s National Deviations 2 Non Invasive Sphygmomanometers Part 1 General Requirements Part 3 Supplementary Requirements for Electro Mechanical Blood Pressure Measuring Systems Part 4 Test Procedures to Determine the Overall System Accuracy of Automated Non Invasive Sphygmomanometers
129. rred Call for service Battery is absent or faulty There is no battery in the monitor Insert a battery The battery is faulty Replace the battery Directions for use Message Device is operating in battery mode Possible cause The AC power cord has been disconnected Troubleshooting 137 Suggested action Touch OK to dismiss or connect the monitor to AC power Configuration Manager messages Message Possible cause Unable to load configuration using A configuration load error occurred factory defaults Functional error Call for service No connection for send A critical configuration load error occurred The monitor is not configured to the network Suggested action Call for service Call for service Call for service Printer messages Message Low battery plug into outlet Printer door is open close to continue Out of paper Printer too hot wait to retry Printer not functional Call for service External device not recognized Printing records Possible cause The monitor s battery voltage is too low to support printing The printer door is open The paper is not properly loaded The paper sensor does not detect paper The print head overheated The printer motor is broken The detection switch malfunctioned Suggested action Connect the monitor to AC power Close the printer door Align the paper with the print head If the problem persists
130. s Be certain that the paper does not catch in the printer door Directions for use Maintenance and service 97 Change the battery Before removing the battery shut down the monitor 1 Turn the monitor upside down to access the battery cover 2 Locate the battery cover indicated by O Insert a coin into the slot and push to open Choose a coin that fits comfortably in the slot 4 Pull the battery out by pulling the battery label which is visible when you open the battery cover 5 Slide in the new battery Ensure that you insert the new battery in the same orientation as the old battery 6 Replace the battery cover by positioning the end below O and then pressing firmly on the opposite end 98 Maintenance and service Note N Welch Allyn Connex Vital Signs Monitor 6000 Series New batteries are approximately 30 percent charged Therefore connect the battery to AC power immediately after inserting a new a battery WARNING Risk of fire explosion and burns Do not short circuit crush incinerate or disassemble the battery pack Never dispose of batteries in refuse containers Always recycle batteries according to local regulations Clean the monitor A A A WARNING Electric shock hazard Before cleaning the monitor disconnect the AC power cord from the power outlet and the monitor WARNING Electric shock hazard DO NOT autoclave the monitor or
131. s SSID Radio band Authentication type Method Security protocol EAP type Identity Password Action Description Enable the radio for device communications When disabled the radio is not available Activate radio network alarms when an alarm condition occurs When disabled radio network alarms are not available Touch ms and enter the service set identifier SSID Enter a maximum of 16 characters Select the radio band Select an authentication scheme Then specify any additional settings that appear Select a method Then touch and enter characters Network key 64 characters or Passphrase 8 to 63 characters Select the security protocol Select the EAP type Enter the EAP identity maximum of 32 characters Enter the EAP password maximum of 32 characters Directions for use Key number Key Configure radio 5 Do one of the following Advanced settings 129 Select the WEP key number Enter the WEP key 10 characters for WEP 64 or 26 characters for WEP 128 Touch Configure radio to activate all new radio settings not selected previously Touch OK in the confirmation popup telling you to power down the monitor Touch the Settings tab Touch the Device tab Touch Power down The radio will reboot Note If you do not touch Configure radio none of the changed radio settings will take effect e _ To continue in the Advanced Settings touch another tab
132. s available to support sending data manually or automatically sending data on manual save The monitor is unable to retrieve a patient list from the network The clinician ID or password is incorrect Suggested action On the Review tab delete old records to prevent the alarm from appearing when new records are saved Power down and restart the monitor If the error persists call for service Take or enter vital signs before saving Call for service Call for service Add a patient ID Delete a patient from the list to add a new patient Stop intervals before changing the patient Call for service Call for service Confirm the clinician ID and password if applicable and retry Directions for use Troubleshooting 135 Radio messages Message Possible cause Suggested action Radio not functional Call for A hardware failure occurred not currently used Call for service service The radio has the wrong software The radio is not connected Radio error Power down and The monitor and the radio failed to establish Power down and restart If restart communication with each other problem persists call for service Unable to establish network The radio is no longer communicating with the Call for service communications Radio out of network range access point Unable to establish network communications Call for service Unable to get an IP address from the DHCP server Call for servic
133. s of connection to the patient A WARNING Patient injury risk Incorrect sensor application or excessive duration of sensor use can cause tissue damage Inspect the sensor site periodically as directed in the sensor manufacturer s instructions While SpO2 is being measured the displayed pulse rate is derived from the sensor If SpO2 is not available the pulse rate is derived from NIBP Detaching the sensor during a measurement in Monitor mode triggers an alarm If SpO2 is being measured continuously on a patient for an extended period change the sensor location at least every three hours or as indicated by the sensor manufacturer s instructions Configure SpO2 alarms Follow these steps to set alarm limits for SpO2 measurements 1 Verify that you are using the Monitor profile which contains the Alarms tab 2 Touch the Alarms tab 3 Touch the SpO2 tab 4 Enter the desired upper and lower alarms limits for SpO2 using the up down arrow keys or the keypad 5 Touch the Home tab The new alarm settings display in the Alarm Limit control button Set SatSeconds limits 1 Touch the Alarm limit control of the SpO2 frame 2 Touch the Alarms tab SatSeconds 3 Touch to select a SatSeconds setting 4 Touch Home to save your settings and return to the Home tab Set Response Mode To set the Response Mode from the Home tab the monitor must be in the Monitor profile Touch AN in the SpO2 frame The SpO2 frame dis
134. screen e Patient information no longer appears at the bottom left of the screen e All controls on the screen are locked except for a on the title bar If you select any area of the screen other than amp a message appears Unlock the display On the locked screen touch and move Slide to unlock located at the bottom right to the rightmost position on the slidebar The following occurs e Patient information appears in the Patient frame e The Navigation area appears e Home tab controls are available for use The display also unlocks when any of the following occur e _ An alarm condition e An externally initiated action such as taking or stopping an NIBP measurement or upgrading software e The monitor powers up 36 Navigation Welch Allyn Connex Vital Signs Monitor 6000 Series 37 Profiles Profiles are variations of the Home tab Each profile gives you access to a different set of features Choose the profile that best suits your needs The monitor offers multiple profiles including Monitor Spot Check and Triage based on the model and any upgrade licenses you purchase Monitor profile The Monitor profile enables you to use alarms and timed intervals It is designed for continuous patient monitoring 10 10 12 31 2011 TEMPERATURE SpHbv T a 8 E 0 1 5 B 6 A INN a 9F 36 69C PATIENT HEIGHT WEIGHT PAIN RR 13579 Adult 72 0 1971 3 15 38 Profiles Welch Allyn Connex Vital Si
135. se 04188 Directions for Use Printed Copy Korean Quick Reference Card 103502 Quick Reference Card English 103658 Quick Reference Card French 103659 Quick Reference Card German 03660 Quick Reference Card Dutch 03661 Quick Reference Card Portuguese 03662 Quick Reference Card Spanish 103663 Quick Reference Card Simplified Chinese 103664 Quick Reference Card Swedish 103665 Quick Reference Card Italian 03666 Quick Reference Card Danish 03667 Quick Reference Card Polish 03668 Quick Reference Card Finnish 103669 Quick Reference Card Greek 103670 Quick Reference Card Norwegian 104330 Quick Reference Card Traditional Chinese 04331 Quick Reference Card Korean Startup Guide 103503 Startup Guide Service Manual English only 103500 Service Manual English 146 Appendix Welch Allyn Connex Vital Signs Monitor 6000 Series Part Number Description Directions for Use ACM Mobile Stand 4800 60 Directions for Use Accessory Cable Management ACM Mobile Stand Warranty Welch Allyn warrants the product to be free of defects in material and workmanship and to perform in accordance with manufacturer s specifications for the period of two years from the date of purchase from Welch Allyn or its authorized distributors or agents The warranty period shall start on the date of purchase The date of purchase is 1 the invoiced ship date if the device was purchased directly from Welch Allyn 2 the date
136. se with Dura Y sensor D YSPD OxiMax PediCheck pediatric spot check use with Dura Y sensor MAX AI OxiMax OxiMax adult sensor single use case of 24 MAX PI OxiMax OxiMax pediatric sensor single use case of 24 MAX II OxiMax OxiMax infant sensor single use case of 24 OXI A N OxiMax Oxiband adult neonatal transducer 1 sensor 50 wraps OXI P I OxiMax Oxiband pediatric infant transducer 1 sensor 50 wraps 142 Appendix SureTemp Plus thermometry Part Number 02895 000 02895 100 02894 0000 02894 1000 05031 101 05031 110 06138 000 Welch Allyn Connex Vital Signs Monitor 6000 Series Description Oral probe and well kit 9ft 2 7M Rectal probe and well kit 9ft 2 7M Oral probe well blue Rectal probe well red Disposable probe covers 1 000 covers packaged 25 box Disposable probe covers 10 000 covers packaged 25 box Temperature calibration key Braun ThermoScan PRO 4000 thermometer and accessory dock Part Number 04000 900 36000 86100 86200 53020 0000 Mounting options Weight scales and connectivity kits Part Number 4800 60 4700 60 4701 62 008 0834 01 Description Dock with thermometer Dock without thermometer Wall mount kit Mobile stand kit Rechargeable battery pack for the thermometer Description Accessory Cable Management ACM organized mobile stand with basket Economy mobile stand with basket Wall mount with basket GCX
137. settings code Touch OK The General tab appears Touch the Data Management tab Touch the Patient IDs tab Specify settings Setting Action Description Name format Select a format for all displayed patient names Full name or Abbreviation Primary label Select the primary identification label for all displayed patients Secondary label Select a secondary identification label for patients A secondary label displays only on the Home tab after the primary label 126 Advanced settings Welch Allyn Connex Vital Signs Monitor 6000 Series Require patient ID to save readings Make entering a patient ID a prerequisite for saving measurements If they fail to enter an identifier the monitor prompts them when they try to save Search by patient ID Enable clinicians to enter a patient ID to query for the patient s information If clinicians scan the ID onto the Home tab or the Summary tab the monitor queries the patient list and the network Returned patient information populates the Patient frame on the Home tab and fields on the Summary tab Clear patient information on manual save Specify that the monitor clears the selected patient after a clinician manually saves measurements from the Home tab Patient information clears from the Patient frame and the Summary tab Note This setting does not take effect when intervals are in progress Retrieve list Enable the monitor to retrieve the patient list from the network When
138. specified during product registration 3 the date of purchase of the product from a Welch Allyn authorized distributor as documented from a receipt from said distributor This warranty does not cover damage caused by 1 handling during shipping 2 use or maintenance contrary to labeled instructions 3 alteration or repair by anyone not authorized by Welch Allyn and 4 accidents The product warranty is also subject to the following terms and limitations Accessories are not covered by the warranty Refer to the directions for use provided with individual accessories for warranty information Shipping cost to return a device to a Welch Allyn Service center is not included A service notification number must be obtained from Welch Allyn prior to returning any products or accessories to Welch Allyn s designated service centers for repair To obtain a service notification number contact Welch Allyn Technical Support THIS WARRANTY IS IN LIEU OF ALL OTHER WARRANTIES EXPRESS OR IMPLIED INCLUDING BUT NOT LIMITED TO THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE WELCH ALLYN S OBLIGATION UNDER THIS WARRANTY IS LIMITED TO REPAIR OR REPLACEMENT OF PRODUCTS CONTAINING A DEFECT WELCH ALLYN IS NOT RESPONSIBLE FOR ANY INDIRECT OR CONSEQUENTIAL DAMAGES RESULTING FROM A PRODUCT DEFECT COVERED BY THE WARRANTY
139. the Patient frame on the Home tab In the Patients tab on the Summary tab clinicians can change the displayed patient type from the default patient type that you set here Tube type Select the number of tubes that are connected to the NIBP cuff that is used with this monitor If you select 1 tube the only algorithm available for selection is Step Unit of measure Select the NIBP unit of measure for display Allow interval program changes Enable clinicians to modify interval program settings from the Intervals tab Algorithm and Cuff inflation target CIT Select the default algorithm used to determine NIBP measurements If you select the Step algorithm touch and enter a default cuff inflation target for each type of patient In the Patients tab on the Summary tab clinicians can change the CITs from the default CITs that you set here 5 Doone ofthe following e _ To continue in the Advanced Settings touch another tab e To exit the Advanced Settings and return to the Home tab touch Exit Specify advanced temperature settings 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab will appear 2 Touch the Parameters tab Touch the Temperature tab 4 Specify settings Setting Action Description Unit of measure Select primary units of measure for the temperature display on the Home tab Display temperature conv
140. the monitor is used exceeds the applicable RF compliance level above the monitor should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the monitor gt Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m Recommended separation distances between portable and mobile RF communications equipment and the monitor The monitor is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or user of the monitor can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the monitor as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m Rated max output 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz ft itt Nr ransmitter eap c 174 P d 2 23 4 P 0 01 0 11667 0 11667 0 23333 116 Guidance and manufacturer s declaration Welch Allyn Connex Vital Signs Monitor 6000 Series Recommended separation distances between portable and mobile RF communications eguipment and the monitor 0 1 0 36894 0 36894 0 73785 1 1 1667 1 1667 2 3333 10 3 6894 3 6894 7 3785 100 11 667 11 667 23 3333 For transmitters rated at a maximum output power not listed
141. this option is selected a Retrieve list button replaces the Add button on the List tab Information from the network populates the List tab when clinicians touch the Retrieve list button Since the Add button is not available clinicians cannot add a patient to the patient list 5 Doone of the following e To continue in the Advanced Settings touch another tab e To exit the Advanced Settings and return to the Home tab touch Exit Specify clinician ID settings Clinician identification appears next to the medicine symbol in the Device Status area on the Home tab 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the Data Management tab Touch the Clinician IDs tab 4 Specify settings Setting Action Description Label Select a type of clinician identification label for display on the Home tab Full name Abbreviation Clinician ID or Symbol only Require clinician ID to save readings Make entering a clinician ID a prerequisite for saving measurements If they fail to enter identification the monitor prompts them when they try to save measurements Clinicians can enter clinician identification on the Clinician tab Search by clinician ID Enable the monitor to query the network for clinician information based on ID The monitor initiates the search when the clinician enters or scans the ID from the Di
142. tial mode 2 kV common mode gt 95 dip in 0 5 cycle 6096 dip in 5 cycles 3096 dip for 25 cycles gt 95 dip in 5 seconds Compliance level 6 kV contact x 8 kV air 2 kV for power supply lines 1 kV for input output lines 1 kV differential mode 2 kV common mode gt 95 dip in 0 5 cycle 6096 dip in 5 cycles 3096 dip for 25 cycles gt 95 dip in 5 seconds Electromagnetic environment guidance Floors should be wood concrete or ceramic tile If floors are covered with synthetic material the relative humidity should be at least 3096 Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment If the user of the monitor requires continued operation during power mains interruptions it is recommended that the monitor be powered from an uninterruptible power supply or a battery Electromagnetic immunity The monitor is intended for use in the electromagnetic environment specified below The customer or the user of the monitor should assure that it is used in such an environment Immunity test IEC 60601 test level Compliance level Electromagnetic environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the monitor including cables than the recomm
143. to its normal layout Close the keyboard Touch one of the following Next Accepts the entry for the current field then clears the field to allow data entry for the next field OK Exits the keyboard and inserts the data Cancel Exits the keyboard without saving entered data Use a barcode scanner The monitor enables the scanning of patients and clinicians barcodes to enter ID information The barcode scanner supports linear and two dimensional barcodes If you haven t done so already attach the barcode scanner to the monitor Use the instructions to attach an accessory Note Refer to the manufacturer s directions for use to ensure that the scanner is set to USB Com Emulation mode Remove the barcode scanner from its holder Hold the scanner approximately 6 inches 15 4 cm from the barcode and squeeze the trigger so that the light from the scanner appears on the barcode Once the scanner completes a successful barcode reading the ID appears in the targeted area Patient frame data field or Device Status area See additional notes below If the scanner has difficulty reading the barcode slowly adjust the distance and the angle between the scanner and the barcode while sgueezing the scanner trigger If it continues to have difficulty verify that the barcode is as flat as possible 46 Using the keypad keyboard and barcode scanner Welch Allyn Connex Vital Signs Monitor 6000 Series Note Note Note You
144. turns WARNING The blood pressure cuff must be properly positioned to ensure blood pressure accuracy and patient safety Wrapping the cuff too loosely preventing proper inflation may result in inaccurate NIBP readings CAUTION f a site other than the bare upper arm is used the blood pressure measurements may be different It is important to document the alternate site on the patient record CAUTION To minimize inaccurate measurement limit patient movement during an NIBP measurement cycle Before taking an NIBP measurement follow these steps to properly attach the cuff to the patient 1 Position the cuff on the patient s bare upper arm midway between the shoulder and the elbow Wrap the cuff snugly so that there is room for no more than two fingers between the cuff and the patient s bare upper arm Position the alignment mark on the cuff directly over the brachial artery Ensure that the blood pressure tubing has no kinks or twists Directions for use Patient monitoring 67 Note In situations where you cannot position the cuff level with the heart you should adjust the measurements as follows for greater accuracy For each inch 2 54 cm that the cuff is above the level of the heart add 1 8 mmHg to the displayed reading For each inch 2 54 cm that the cuff is below the level of the heart subtract 1 8 mmHg from the displayed reading It is important to document the adjustment on the patient record NIBP measurem
145. uching the screen Home tab The Home tab includes the following areas 12 29 2013 Continuous Ay G ans TEMPERATURE PATIENT 13579 Item Area 1 Device Status 2 Content 3 Navigation Device Status area 6 09 16 12 31 2011 The Device Status area located at the top of the Home screen displays the following monitor information from left to right e Clinician identification The format can be a name ID number or icon Touch this area to navigate to the Clinician login e Device location 32 Navigation Welch Allyn Connex Vital Signs Monitor 6000 Series e Time and date Touch this area to navigate to date and time settings e Connection status wired or wireless The icons indicate which connection type if any is currently active Icon Connection type Ethernet n E USB V Wireless Blank No connection e Process indicator This indicator appears when system or patient data is transferred between the monitor and the network Battery condition Estimated battery capacity is displayed in hour s minute s format This area also provides e Interactive alarm and information messages e Shortcuts to some setting controls For example touching the Alarm icon displays the Alarms tab Battery status The battery status indicator displays the state of the battery The battery status is represented by icons in the right corner of the Device Status area e The monitor is connected to a
146. uration range 0 to 25 g dL Masimo SpHb sensor accuracy guide Adults Pediatrics no motion 8 to 17 g dL 1 g dL SpHb accuracy has been validated on healthy adult male and female volunteers and on surgical patients with light to dark skin pigmentation in the range of 8 to 17 g dL SpHb against a laboratory co oximeter This variation equals 1 standard deviation which encompasses 68 of the population The SpHb accuracy has not been validated with motion or low perfusion Environmental specifications Operating temperature 50 F to 104 F 10 C to 40 C Storage temperature 4 F to 122 F 20 C to 50 C Operating altitude 557 to 10 000 ft 170 m to 3 048 m Operating humidity 15 to 95 noncondensing Storage humidity 15 to 95 noncondensing Monitor radio The monitor s radio operates on Welch Allyn FlexNet or other 802 11 networks 106 Specifications Wireless network interface Frequency Channels Security encryption authentication Antenna Wireless data rates Agency approvals Protocols Data transfer protocols Modulation Output power Ancillary IEEE standards Welch Allyn Connex Vital Signs Monitor 6000 Series IEEE 802 11 b g 802 11a 802 11 b g 2 402 GHz to 2 4835 GHz 802 11a 5 125 GHz to 5 875 GHz Up to 14 in 802 11b g up to 24 in 802 11a country dependent WPA2 AES either EAP or PSK authentication Internal multiband PIFA 802 11b 1Mbps or higher during vitals transmission only 802
147. used A Alarm active Directions for use Screen elements 7 Patients list and review List Summary Modifiers Manual Diacritical marks key Symbols key AEL available for languages that use diacritical marks appearance differs based on language Send patient test reports aM Print patient test reports Cancel print reguest Add patient identifiers Retrieve the patient list from the network Save configuration settings Advanced settings eno R Save to USB flash Configure from USB Sa p USB drive onfigure from USE flash drive Restore factory All setti default settings 8 Screen elements Welch Allyn Connex Vital Signs Monitor 6000 Series About warnings and cautions Warning and caution statements can appear on the monitor on the packaging on the shipping container or in this document The monitor is safe for patients and clinicians when used in accordance with the instructions and the warning and caution statements presented in this manual Before using the monitor familiarize yourself with the sections of this directions for use that pertain to your use of the monitor e Failure to understand and observe any warning statement in this manual could lead to patient injury illness or death e Failure to understand and observe any caution statement in this manual could lead to damage to the equipment or other property or loss of patient data General
148. ve been sent to the network You can configure some profiles and settings to automatically send measurements to the network Patient measurements older than 24 hours are automatically deleted from the patient records list on the Review tab The date and time stamps on saved patient measurements will adjust in response to new date and time settings 1 Touch Review from the Home tab 2 Touch m next to the names of the patients whose data you want to print Once selected a check mark will be added to the box 3 Touch Print v 4 Confirm the number of records you want to print and touch OK The data is sent to the printer A CAUTION Verify patient identity on the monitor after manual or barcode entry and before printing or transferring patient records Printer The monitor prints to a strip to create printouts of patient information and data Note The sample printouts below are English but the language in the printouts is defined by the language selected on the monitor 50 Patient data management Welch Allyn Connex Vital Signs Monitor 6000 Series ON Patient ID 13579 ID 13579 Room Bed Room Bed Clinician Clinician 12 31 2011 amp 08 53 SYS DIA MAP PR Sp02 Temp mmHg BPM 2 F SYS 106 mmHg pone D UR DUNS IUE DIA 68 mmHg 12 31 2011 07 46 MAP 81 mmHg 78 9 PR 71 BPM 12 31 2011 amp 07 46 Sp02 86 55 65 78 97 97 oF 12 31 2011 07 46 ee i cm 110 71 84 82 97 Weight 68 0 kg
149. ve changed and saved will be maintained at the next startup Note Because power is still available to charge the battery and power the monitor the monitor is in Standby mode Reset the monitor If the monitor stops functioning you can press and hold My for approximately 6 seconds to allow the hardware to completely cycle off and to reset the monitor configuration settings to the last saved default power up configuration The button is located on the side of the monitor AN CAUTION Do not use a long press of ZO to power down the monitor when it is functioning normally You will lose patient data and configuration settings Note Because power is still available to charge the battery and power the monitor the monitor is in Standby mode Set the date and time 1 Touch the Settings tab 2 Touch the Device tab 3 Touch the Date Time vertical tab 30 Startup 4 Welch Allyn Connex Vital Signs Monitor 6000 Series To change the date and time values Touch the up and down arrow keys or touch and enter a value Repeat for each value you want to change Note The date and time stamps on saved patient measurements will adjust in response to new date and time settings Enter clinician information 5 Set the def Go to the Clinician tab using one of these methods e On the Home tab touch the Clinician ID section of the Device Status area top left corner of the screen e Touch the Settings gt Clinician tab
150. ved from the SpO tab in the Alarms tab Specify the minimum amount of time that an SpHb alarm condition must be active before audio and visual signals occur e _ To continue in the Advanced Settings touch another tab e To exit the Advanced Settings and return to the Home tab touch Exit Specify advanced display settings 1 Access the Advanced Settings a Touch the Settings tab b Touch the Advanced tab c Enter the Advanced settings code d Touch OK The General tab appears 2 Touch the Display tab Specify settings Setting Display lock Display power saver Device power down 4 Doone ofthe following Action Description Specify the required period of clinician inactivity before the touchscreen locks Specify the required period of monitor inactivity before the display turns off Clinician interactions new vital sign measurements or alarm conditions automatically turn on the display Specify the required period of monitor inactivity before the monitor turns off e _ To continue in the Advanced Settings touch another tab e _ To exit the Advanced Settings and return to the Home tab touch Exit 120 Advanced settings Welch Allyn Connex Vital Signs Monitor 6000 Series Specify a monitor location You can associate the monitor with a specific location The location appears in the Device Status area 1 Access the Advanced Settings a Touch the Settings tab b Touch th
151. when an alarm condition is active brief press e Resets the monitor and sets the monitor into Standby mode press and hold for 6 seconds A CAUTION Do not use a long press of ZO to power down the monitor when it is functioning normally You will lose patient data and configuration settings The LED in the center of the power plug symbol indicates the battery charging status e Green indicates that AC power is present and that the battery is fully charged e Amber indicates that AC power is present and that the battery is charging The monitor has distinct power states Monitor on The monitor is operating on battery power or AC power You can utilize the monitor s features and the display is active Display power saving The monitor is operating on battery or AC power but the display is off to conserve power A brief press of the power button sets the monitor into Display power saving 28 Startup Welch Allyn Connex Vital Signs Monitor 6000 Series mode from the active state Settings for this mode can be changed in the Advanced Settings Display tab Battery powered accessories connected to the monitor continue to charge while the monitor is in this mode and connected to AC power Note The monitor will not enter the Display power saving mode while an alarm condition is active or when NIBP intervals are in progress In addition the monitor will exit this mode if an alarm occurs The following actions

Directions for use, Welch Allyn Connex® Vital Signs Monitor 6000

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Directions for use, Welch Allyn Connex&reg; Vital Signs Monitor 6000

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Directions for use, Welch Allyn Connex® Vital Signs Monitor 6000