CONTEC08A users` manual
Contents
1. level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol 6 NOTE 1 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 A 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 the CONTECOSA is used exceeds the applicable RF compliance level above the CONTECOSA should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as reorienting or relocating the CONTECOSA B Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT or SYSTEM for EQUIPMENT or SYSTEM that are not LIFE SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and th2. take the thick clothes off instead of rolling up the sleeves In order to measure accurately pay attention to applying the cuff properly left arm Make sure the air plug is securely inserted in the main unit 2 Stretch cuff into a barrel for the arm can conformable enter into the barrel TE 8 Arm penetrate throught the cuff the air tube of the cuff will pass the top of your palm 4 Apply the cuff to your upper arm The color marker is on the inside center of your arm and make the air tube aligned with your middle forger The bottom of the cuff should be approximately 2cm 3em above your elbow 6 Be fixed with cloths and wrapped tight cuff the arm and the cuff should not have gaps Chapter10 BP Measurement 10 1 Accurate Measurement Way Measurement in quiet and relaxing state 1 Place your arm on a table Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 ch be 2 The cuff is level with your heart 3 The palm of the hand is up and the body relax Try to measure your blood pressure at the same time each day with the same arm and the same pose for consistency The high and low location of cuff will cause changes in measurement results Do not touch Electronic Sphygmomanometer cuff and windpipe during measurement Measurements should be taken in a quiet place and the body relax Remain still 4 5 minutes before measurement Relax the body do not let the muscle activity Do no
3. time from 00 00 00 set the date and time again The Electronic Sphygmomanometer stores the measure results of three users automatically and up to 100 items for every user The results can be uploaded to PC via USB and processed with the PC software If the date and time are set correctly the date and time when measuring will be correct in the memory otherwise it may not be correct AN Note AN Correctly use data upload function 1 Turn on the device to enter the main interface shown as the follow 06 19 2009 12 30 30 Ml 6 19 2009 12 30 30 USER USER2 MENU MEMORY 2 Press MENU button to enter SYSTEM MENU and select SYSTEM TIME item in system menu The current time will be displayed 06 19 2009 12 30 30 iFFA 06 19 2009 12 30 30 FFA SYSTEM TIME SYSTEM SETUP ENTER DATE SYSTEM TIME ENTER 06 19 2009 DELETE DATA ENTER TIME 12 30 30 ALARM SETUP ENTER EXIT CONFIRM EXIT ENTER UP ENTER DOWN 3 Press UP or DOWN buttons to set date and time 4 After setting select CONFIRM item and press ENTER button to confirm the setting value If you do not want to change the time select EXIT item and press ENTER button to return the previous menu AN Note AN Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Please choose the computer which should be ensured compliance with the reguirements of IE C609320 or else it may damage the devi
4. EXE 4 Follow the instructions in the screen Refer to Software Help for details about the operation method of the PC software Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter17 Keys And Symbols Signal Description Warning See User Manual gt SYS Systolic pressure MAP MAP pressure DIA Diastolic pressure Pulse rate bpm ADU Adult PED Pediatric NEO Neonatal INFO Information Open the alarm sound indication Close the alarm sound indication Low power Full power 1 no NIBP data to review 2 n0 finger inserted to SpQ probe 3 An indicator of signal inadequacy Class equipment WEEE 2002 96 EC BF Applied Part Serial number C This item is compliant with Medical Device Directive 93 42 EEC of June 0123 14 1993 a directive of the European Economic Community European Representative USB or connect SpO probe Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter18 Error Message Error message will be displayed in the screen if there is something wrong when measuring The causes and solutions are shown as follows Self test failure Function abnormal Please contact us System failure Cuff is not connected Loose cuff Correctly connect cuff refer to 8 page correctly Make sure the cuff plug is securely Air leakage Cuff plug fall off inserted in the windpipe refer to 8 page The
5. FF button to clear up the audio alarm 4Vake off the cuff hold ON OFF button to turn the device off The device will automatically turn off after two minutes in which there is no operation to the device even if you forget to turn the power off Chapter11 Memory Function The devicer is designed to store and display the blood pressure pulse rate values and the date and time when measured which are up to 100 items If there have been 100 items stored when the 101 measurement have been taken the earliest results are deleted 11 1 Review The Memory Value 1 In the main interface interface when boot strap press MEMORY button to review the most recent measurement values in large print with the serial number from 1 to 100 06 19 2009 12 30 30 LAMA USER 01 TOTAL 50 NO0 03 TIME 06 19 2009 12 30 2 Press UP DOWN button to circularly switch the former measurement values The right figure shows that there is no Measurement result 3 Press LIST button to switch to data table interface Henrotech nv Acacialaan 8 2630 Aartselaar amp 06 19 2009 12 30 30 LIHA BP TABLE NO SYS DIS PR MAP 03 125 84 53 94 2009 06 19 12 30 02 116 77 78 089 2009 06 19 12 30 01 175 108 77 131 2009 06 18 12 30 TREND T 03 844 53 33 06 19 2009 12 30 30 Fall USER 01 TOTAL 50 N0 03 TIME 06 19 2009 12 30 EXIT LIST DOWN www henrotech be 4 Press TREND button
6. Hg Electronic Sphygmomanometer CONTECOSA 2 8 color LCD Display Resolution Pressure Measurement Accuracy Cuff Pressure Accuracy 3mmHg The BP Value of the device is equivalence with the measurement Error value of Stethoscopy The error meets all the conditions in the pa ANSI AAMI SP 10 2002 A1 2003 A2 2006 Operating 5 C 40 C 15 RH 80 RH Transport and Storage 20 C 55 C lt 95 RH SOKPa lO5Ka 4 AA alkaline batteries AC Adapter separately sold 30 L 11000 80mm Main Unit Weight 300gram Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Accessories Standard Configure Adult Cuff limb circumference 22 32cm middle of upper arm Software CD User Manual USB data line four AA alkaline batteries Separate Sale Pediatric Cuff limb circumference 10 19cm middle of upper arm Neonatal Cuff limb circumference 6 llcm middle of upper arm AC Adapter Input AC 100 240V 50 60Hz AC500mA Output DC 6 0V Z 1 0A Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter22 SpO Specification Name SpO Probe Accessory Separate Sale Model Y 1OUCH150 SpO Measuring Range 0 100 Pulse Rate Measuring Range 30bpm 250bpm 70 100 2 0 69 undefined pulse filling ratio SpO error 0 4 pulse rate error Measurement Range Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www
7. OSA can continue the operation during power mains interruptions due to the usage of battery Mains power quality should be that of a typical commercial or hospital environment www henrotech be Guidance and manufacturer s declaration electromagnetic immunity for EOUIPMENT and SYSTEMS that are not LIFE SUPPORTING Guidance and manufacturer s declaration electromagnetic immunity The CONTECOSA is intended for use in the electromagnetic environment specified below The customer or the user of CONTECOSA should assure that it is used in such an environment Compliance Immunity test IEC 60601 test level level Electromagnetic environment guidance eve Portable and mobile communications equipment should be used no Sian to any part of the CONTECOSA including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance Conducted RF OV ins 35 IEC61000 4 6 150 kHz to 80 MHz d P 1 Radiated RF 3 V m E 5 IEC61000 4 3 80 MHz to 2 5 GHz d s 60 MHz to 800 MHz 1 d Ee 800 MHz to 2 5 GHz 1 Where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in metres m Field strengths from fixed RF transmitters as determined by an electromagnetic site survey should be less than the compliance
8. ce Chapter7 Unit There are two units mmHg and kPa The default is mmHg To switch mmHg and kPa units enter the SYSTEM SETUP submenu in SYSTEM MENU and complete switching in UNIT item 06 19 2009 12 30 30 CFA 06 19 2009 12 30 30 CFA SYSTEM SETUP a 2 SYSTEM SETUP LANGUAGE ENG SYSTEM TIME ENTER UNIT DELETE DATA ENTER USER PURVIEW ALL ALARM SETUP ENTER MEASURE MODE ADU EXIT EXIT ENTER 4 ENTER Chapter8 User Switch The Electronic Sphygmomanometer stores the measure results of three users automatically and up to 100 items for every user Press USER button in main interface to switch users Or press USER PURVIEW item in SYSTEM SETUP menu to switch users amp 06 19 2009 12 30 30 LUHA 06 19 2009 12 30 30 Hall e SYSTEM SETUP ENTER LANGUAGE ENG SYSTEM TIME ENTER UNIT mmHg DELETE DATA ENTER USER PURVIEW ALL ALARM SETUP ENTER MEASURE MODE ADU SYSTEM SETUP EXIT EXIT ENTER ENTER AN Note AN When the USER PURVIEW isset tobe ALL current user can be switched under main interface when set to a certain user it will not be able to switch Chapter9 Applying the Arm Cuff The measurement can be carried out by applying the cuff on left or right arm Remove tight fitting clothing from your upper arms Carry out the operation in a room with comfortable temperature Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be When measuring
9. ce A The internal components and cables should not be changed as this may decreased IMMUNITY of the device A The Electronic Sphygmomanometer should not be used adjacent to or stacked with other equipment Classification EMC Group I Class B According to the MDD 93 42 the classification of this medical device La The type of protection against electroshock Class equipment The degree of protection against electroshock type BF applied par ENI The degree of protection against ingress of water IPX0 According to the mode of operation Continuous According to the degree of safely of application in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter21 NIBP Specification Name Model Display NIBP Specifications Measurement Method Oscillometric method Working modes Automatic 0 290mmHg 0 38 6kPa Pressure 0 235mmHg 0 31 3kPa Measurement Range E 0 140mmHg 0 18 6kPa Pulse 40 240 min Inflation 120mmHg Tommi SYS ALM 40 270 mmHg adult mode DIA ALM 10 215 mmHg M SYS ALM 40 200 mmHg Alarm Range pediatric mode DIA ALM 10 150 mmHg SYS ALM 40 135 mmHg neonatal mode DIA ALM 10 100 mmHg Overpressure protect 240 SmmHg Imm
10. e CONTECOSA The CONTECOSA is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the CONTECOSA can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the CONTECOSA as recommended below according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter Rated maximum m output power of 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz transmitter For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be estimated using the equation applicable to the frequency of the transmitter where P is 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 Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be
11. es with new Hold the on off exhausted ones button but can not _ _ Check the battery installation for The battery polarities is start the device proper placement of the battery reversed polarities Cuff inflation start before press the measurement Pull out the cuff to deflate Stop using button or never stop inflating when measuring the device and contact us Pull out the cuff to deflate Stop using Cuff never deflation the device and contact us No deflation or deflation error Pull out the cuff to deflate Stop using Air pressure error or inflation without stop the device and contact us Keep arm body still measure again No press value displayed or the value unchanged or Pull out the cuff to deflate Stop using change erratically when cuff inflated the device and contact us Switch on the power once again and restart an operation Other phenomenon Replace the batteries If no please contact us Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter20 Clean And Maintenance Please follow the instructions in the user manual If you do not comply our company will not assume responsibilities of the quality MW Frequently clean the Electronic Sphygmomanometer MW If there is something dirty on the device clean it with a soft dry cloth MW ff the unit is particularly dirty you can clean it with a soft cloth dampened with water or neutral detergent after
12. flect the cuff and the air tube forcibly This device is intended for using in measuring blood pressure and pulse rate in the adult pediatric and neonatal population A Warning A Please use the device on the adult object who can read the user manual and the error message shown on the screen Read the user manual before use the device in order to take actions according to the manual when something wrong with the device For pediatric and neonatal population measurement should be only performed by gualified personnel And please make sure to select the right user mode and cuff before use Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter2 Main Unit The production is in the package Open the package and confirm whether the production is whole Display Cuff Plug Cuff Air Plug UP DOWN Button MEMORY Button AC Adapter Jack MENU Button USER SWITCH Button USB Plug Jack ON OFF Button START STOP Button O O O O Accessories Adult Cuff Dry Battery Specification limb circumference 22 32cm middle part of upper arm please choose suited cuff when measuring pediatric or other USB Data Line Software CD User Manual AC Adapter InputAC 100 240V 50 60Hz AC 500mA Output DC 6 0V 1 0A SpO Probe Y10UCH150 SpO Measurement Range 35 100 Measurement Accuracy 70 100 2 T 03 844 53 33 www henrotech be Pulse Measurement Range 30 250bpm Cha
13. flow during NIBP measuring may adversely affect the reading of SpO value AN Note AN Make sure the nail covers the light window Othe wire should be on the backside of the hand OSpO value is always displayed in the fixed place Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be A Warning AY OCheck if the sensor cable is in normal condition before monitoring After unplugging the SpO probe cable from the socket the interface will return ODo not use the SpO probe once the package or the sensor is found damaged Instead you shall return it to the vendor Prolonged and continuous monitoring may increase jeopardy of unexpected change of dermal condition such as abnormal sensitivity erubescence vesicle repressive putrescence Particularly in newborns or in a Perfusion disorders and changes or immature skin form of the patient According to skin quality change correct optical path alignment and attachment methods to regularly check the place of SpO probe and change the attachment position when the quality of skin decline More frequent examinations may be required for different patients Chapter14 Monitoring Procedure 1 Attach the sensor to the appropriate site of the natient finger as following figure i i G place SpO 2 Plug the connector of the SpO probe cable into the USB socket in the lower right of the device The main interface will switch to SpO interface The update pe
14. henrotech be Appendix Guidance and manufacturer s declaration electromagnetic emissions for all EOUIPMENT and SYSTEMS Guidance and manufacturer s declaration electromagnetic emission The CONTECOSA is intended for use in the electromagnetic environment specified below The customer of the user of the CONTECOSA should assure that it is used in such and environment Emission test Compliance Electromagnetic environment guidance RF emissions The CONTECOSA uses RF energy only for its CISPR 11 Group 1 internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment The CONTECOS8A is suitable for use in all CISPR 11 establishments including domestic Harmonic emissions establishments and those directly connected to the public low voltage power supply network Voltage fluctuations that supplies buildings used for domestic flicker emissions Complies purposes IEC61000 3 3 Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Guidance and manufacturer s declaration electromagnetic immunity for all EOUIPMENT and SYSTEMS Guidance and manufacturer s declaration electromagnetic immunity The CONTECOSA is intended for use in the electromagnetic environment specified below The customer or the user of CONTECOSA should assure that it is used in such an environment A Electromagnetic environment Im
15. munity test IEC 60601 test level Compliance level guidance Electrostatic discharge ESD IEC 61000 4 2 Electrical transient burst IEC 61000 4 4 Surge IEC 61000 4 5 Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 Power 50 60Hz field IEC61000 4 8 frequency magnetic 6 kV contact 8 kV air 2 kV for power supply lines 1 kV differential mode 2 kV common mode lt 5 Ur gt 95 dip in Ur for 0 5 cycle 40 Ur 60 dip in Uz for 5 cycles 70 Ur 30 dip in Ur for 25 cycles lt 5 Ur gt 95 dip in Ur for 5 sec 6 kV contact 8 kV air 2kV for supply lines power kV differential mode 2 kV common mode lt 5 Ur gt 95 dip in Ur for 0 5 cycle 40 Ur 60 dip in Uy for 5 cycles 70 Ur 30 dip in Ur for 25 cycles lt 5 Ur gt 95 dip in Ur for 5 sec NOTE Uris the a c mains voltage prior to application of the test level Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 Floors should be wood concrete or ceramic tile If floor are covered with synthetic material the relative humidity should be at least 30 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 The CONTEC
16. n v HENROTECH s a Respiratory Care CE on User Manual Electronic Sphygmomanometer Model CONTECOSA CONTEC apa m To assure the correct use of the product safety measures please carefully read user manual before using m After reading please validly keeping to refer and consult at any moment Contents Chapterl Safety Precautions errrrnrrnnennnnennnneneeeeeeeeeeennnnnn enne nene eeeeeeeeeeeennnnnan anne eeea 1 Miter VE ari EENET N t 3 Chapei Buon UnC ONS A am 4 Chape Eximia Mert eS e s E E 4 Chapters Dry Battery AC Adapter Installation rrrrrrnnennnteeeeeeeeeenennennnnn nene 5 2 Dry Batory motala Osas enn a 5 5 2 Using The AC Adapter rrrrrnnenennneeeeeeeeeeeenennnen nene n nn neeeeeeeeeeneennnnann enne 5 Chaptero Sette The Date And TIME orreri ston ern n ea Esai aE 6 hane L a A E E A E 7 110 30 MAD mie ea E O E mre ery verter Tre rr ere 7 Chapter Applying Me Arm C UTi session ieaie OOE E ir 7 Chaperio IBF IVICA IE 19755 01 ser DE 8 10 1 Accurate Measurement Way 4 snvnrreeeeeennnnnnnoeeeeennn enn noeeenennn nne nneeeeeenan nne neeeeeenennnea 8 I BEMO U NIN a a peacou as sedaanananeeonetardeacoeass 9 Chapterl Memory Function F KN A cccccccccsseesssssssssssseeeeeceecsseeseeeeessssees 10 11 1 Review The Memory Valug SRPMRBMIMMIET 5y ccccccccccccccccccsseecssssssssessseeeeseceeeeeeeees 10 112 Delete Memo
17. o enter system menu select ALARM SETUP item to enter its interface and then set alarm on off and the high and low alarm limits when blood pressure is Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be higher than the high limit or lower than the low limit the physiological alarm will occur 06 19 2009 12 30 30 FM 2009 06 19 12 30 30 Fall ALARM SETUP 4 ALARM OFF SYS ALM HI mg 140 SYS ALM LO mmHg 90 DIA ALM HI mmHg 90 DIA ALM LO mmHg 40 DEFAULT NO SYSTEM SETUP ENTER SYSTEM TIME ENTER DELETE DATA ENTER ALARM SETUP EXIT ENTER ENTER DOWN Press any button to cancel the alarm in physiological alarm state and this method brings no affection to the next alarm To close alarmin ALARM SETUP will disable the alarm function until switch alarm on Technical Alarm When power is about to exhaust and alarm is on then the alarm will occur This alarm can not be cancelled unless being closed or the power replaced Chapter13 SpO Measurement Function Separate Sale Please pay attention to A Warning AY Pulse oximeter can overestimate the SpO value in the presence of Hb CO Met Hb or dye dilution chemicals ES Electrosurgery equipment wire and SpO cable must not be tangled up Do not put the sensor on extremities with arterial catheter or venous syringe Do not perform SpO measuring and NIBP measuring on the same arm at one time because obstruction of blood
18. pter3 Button Functions All the operations to the Electronic Sphygmomanometer are through the buttons The names of the buttons are above them They are ON OFF Hold the button to start or close the device m START STOP Press to inflate the cuff and start a blood pressure measurement When measuring press to cancel the measurement and deflate the cuff al ES The three buttons correspond with the hint in the LCD screen downside pressing any button will carry on corresponding function eg MENU ENTER LIST etc A Up and down buttons respectively carry on the functions of moving the cursor up and down changing the parameters and switching the status Chapter4 External Interfaces AN Note AN Please hold the air plug to remove the NIBP cuff Cuff Socket left side The right side of the instrument is USB socket and AC adapter socket AUSB socket 2AC adapter socket right side Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be ChapterS Dry Battery AC Adapter Installation The production can use dry battery or AC adapter as power source 5 1 Dry Battery Installation 1 Press the Aindicator on the battery cover and slide the cover off in the direction of the arrow 2 Install 4 AA size dry batteries so the positive and negative polarities match the polarities of the battery compartment as indicated 83 Replace the battery cover Icon d4 h the ba
19. pulse signal is too weak Weak signal Correctly connect cuff refer to 8 page or the cuff is loose Cuff is blocked or squeezed Correctly connect cuff refer to 8 page The signal extent 15 too big Excessive movement owing to the arm or body Over range moving or other reasons when Saturated signal Keep arm body still measure again measuring It takes too much time Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter19 TROUBLESHOOTING Abnormal l Causes Solutions Phenomenons Correctly connect cuff refer to 8 Cuff is not connected correctly page BP measurement Talk or move arms when values too high or Keep quiet and restart a measurement measuring too low l l The turnup clothing presses the Take off the clothing which presses arm the arm and restart a measurement Cuff leakage Buy a new cuff The cuff windpipe is not No pressure Correctly connect correctly connected with cuff Cuff is not inflated Stop using the device and contact us Loose cuff Correctly apply cuff Cuff deflates in short time It can not carry on measurement when press the Switch on the power once again and measurement button restart a measurement No use for a long time the Power off suddenly power of batteries can be Replace all four batteries with new when inflating exhausted owing to the ones changed temperature Power of batteries can be Replace all four batteri
20. riod of data is less than 5 seconds which is changeable according to different individual pulse rate This operation brings no affection to other functions A Warning AN Uncomfortable or painful feeling may appear if using the device ceaselessly especially for the microcirculation barrier patients It is recommended that the sensor should not be applied to the same finger for over 2 hours 06 19 2009 12 30 30 Hall 6 19 2009 12 30 30 PR 9 USER2 MENU MEMORY Measurement Limitations During operation the accuracy of oximeter readings can be affected by High frequency electrical noise including noise created by the host system or noise from external sources such as electrosurgical apparatus connected to the system Intravascular dye injections Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Excessive patient movement External light radiation Improper sensor installation or incorrect contact position of the patient SpO probe temperature optimal temperature between 28 C and 40 C Placement of the SpO probe on an extremity that has a blood pressure cuff arterial catheter or intravascular line Significant concentrations of dysfunctional hemoglobin such as carboxyhemoglobin and methemoglobin SpO gt too low Bad circular injection of the part being measured It is required to use SpO probe which is provided by our company contact with o
21. ry Vat CS JE eae aieiateatea a ba eesadisssnarnsdidhecubawbaciebadalnawadscebsantecons 11 Chapter12 Alarm Functing SES JA 0 E a PP kk ccc cece cccceseeeeeseesees 11 Chapter13 SpO2 Measurement Function Separate Sale eeeeneneeeeeeeeeeeeeeenennnn nene 12 Chapter14 Monitoring Pe ebdue get 1 CA Be ee A M Tee ee Dee occ cccccccccccccccccceseeeeesessees 13 Chapters Maintenance and CARIN piss stscscacet asses amaan aata namah aaa 14 Chapterl6 Installation Of The Software omsnsnas e v tta akkadi kaa kaak kajaki kapa jaaa 15 TO Demand Oidi III Ia 15 16 2 Tas A TAGA OF 5 OHM AEG iii saatana EENEN EN EEE E EEN ENES EEA NAN EARE aatal 15 Chapter17 Keys And SymbOls merrrennnnnnnnnnnnnneeeeeneveeeennann arenen nneeeeeeeeeeeeenennnnn naene 16 Chamero Eror M Ie 17 Chapteri9 TROUBLESHOOTING aia iaa E asa alal 18 Chapter20 Clam And Mamten ane sssssrossc riproi roan E akkas OnE E 19 Chapter21 NIBP Speci GAO jae stat osakaal anal ama OE rE rO O E Onie eSa Operai eti 21 Chapier 2 SPO Sp eC iC Al Ol ossee nr aE ES ENE a EREE 23 Appendix AM mm M i sinew tagnsiandaniiane 24 Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapterl Safety Precautions Before use carefully read Safety Precautions for a correct use To prevent users suffered hurt or damnification due to improper use see Safety Precautions and use this product properly For safe
22. t talk and movement during the measurement Wait 4 5 minutes between measurements Do not use a cellular phone near the device 10 2 BP Measurement OPress START STOP button to take a measurement 06 19 2009 12 30 30 FAA 06 19 2009 12 30 30 LUHA PRESS SYS START STOP v E INFO DIA USER O3RECORD PR USER2 USER2 MENU MEMORY Start measurement measurement result During measurement please keep correct pose and quiet state do not move Stop Measurement During measurement if you wish to stop measuring press START STOP button to stop and deflate Confirm Measurement Value Measurement value can be automatically stored using memory function refer to 10 page Self diagnosis and treatment using measured results may be dangerous Follow the instructions of your physician A Note A E Wait 4 5 minutes between measurements When repeated measurements because the arm appears congestion it may not get correct blood pressure measurement After the blood flow take a measurement once again E When some factors affect the measurement results in measurement process error messages Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be hints will appear on the screen you can obviate the malfunction and restart a measurement Oln no physiological alarm state press any button to carry on the corresponding button function in audio alarm state press any button except ON O
23. the cloth can be full twisted A Warning AY Do not submerge the device in water AN Advice AN E Do not use any naphtha thinner or gas to clean E Do not attempt to clean or wash the cuff Keeping AY Advice AY Do not place the machine in the following areas HW Easy to splash water areas MW Direct sunlight extreme hot humidity dust causticity gas areas Ww Lean or the area which can cause vibration impact LES 4 l J x HW Chemicals or corrosive gas storage areas E Remove the batteries if the unit will not be used for long time A Warning A It is recommended that you check if there is any damage on the Sphygmomanometer or the accessories regularly if you find any damage stop using it and contact our Customer Service immediately In addition the overall check of the Sphygmomanometer including the NIBP calibration Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be and safety check such as the leakage current should be only performed by gualified personnel once every 12 months A Warning AY The disposal of scrap instrument and its accessories and packing including batteries plastic bags foams and paper boxes should follow the local laws and regulations EMC declaration A When this device is installed or putted into service EMC should be paid more attention as the portable and mobile RF communications equipment with higher EM interference can affect this devi
24. to display trend interface SYS diff H DIA SYS DIA 2009 06 18 2 2009 06 19 EXIT MEMORY 5 Finish displaying the measurement values Press EXIT to return the main interface or hold ON OFF button to turn the power off The device will automatically turn off after two minutes in which there is no operation to the device even if you forget to turn the power off 11 2 Delete Memory Values Users can delete all values stored in the memory of each user separately instead of deleting a special item 1 Press MENU button to enter SYSTEM MENU select DELETE DATA item and enter its interface in which select the user whose data will be deleted All measurement results of selected user will be deleted after confirm 06 19 2009 12 30 30 FM 06 19 2009 12 30 30 FM 06 19 2009 12 30 30 Fall DATA DELETE SYSTEM SETUP ENTER USER 1 SYSTEM TIME ENTER V USER 2 E DELETE DATA ENTER USER 3 ARE YOU SURE TO DELETE ALARM SETUP ENTER THE DATA OF ALL USER USER 2 EXIT LOK ENTER 2 Finish Operation Select CONFIRM or EXIT to return the previous menu or hold ON OFF button to turn the power off The device will automatically turn off after two minutes in which there is no operation to the device even if you forget to turn the power off Chapter12 Alarm Function Alarms are classified into two categories technical alarm and physiological alarm Physiological Alarm User can press MENU button t
25. tteries power will exhaust Replace with four new batteries the same sort at the same time Turn the unit off before replacing the batteries AN Note AN Dispose of the batteries according to applicable local regulations about environmental 5 2 Using The AC Adapter Connect device and the AC Adapter Insert the AC Adapter Plug into the AC Adapter Jack on the right side of the device 2 Plug the AC Adapter into a AC outlet AN Note AN Hold and pull the Housing to remove the AC Adapter from the electrical outlet Do not remove by pulling on the cord 2 Remove the AC Adapter plug from the unit Please be sure to use dedicated AC adapter AN Note AN Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be You d better take off batteries when use the AC adapter as power source If there is any damage to the AC adapter you should use batteries to run the device When adapter and batteries are both used at the same time the battery power will not be consumed Switch adapter and battery as power supply when the device is off otherwise the device may shutdown due to power failure Chapter6 Setting The Date And Time It is necessary to set date and time after turning on the device The Electronic Sphygmomanometer automatically stores measurement results with date and time If dry battery power exhausts or removed then after the device turned on the date resumes from the last setting value and the
26. ty reasons be sure to comply with safety precautions AN Note AN If not to use correctly it exists that a potentially hazardous situation which may result in injury to the user or patient or damage to the equipment or other property AN Note AN Self diagnosis and treatment using measured results may be dangerous Follow the instructions of your physician Contact your physician for specific information about your blood pressure Please hand measurement results to the doctor who know your health to accept diagnosis For severe blood circulation disorder or arrhythmia patients please use the device under the guidance of a doctor Otherwise it may lead to acute hemorrhage or measurement error as a result of squeezed arm This device is intended for using in measuring blood pressure and pulse rate Do not use for any other purpose Otherwise it may cause accident or holdback Please use special cuff Otherwise it is possible that measurement result is incorrect Do not disassemble or attempt to repair the unit or components without permission Otherwise it can not measure correctly Operation for AC Adapter Separate Sale AN Note AN Please use sold separately dedicated AC adapter Otherwise it may cause trouble Sold separately dedicated AC adapter be sure to use a separate socket Otherwise it may cause electric shock or injury When there is breakage of sold separately dedicated AC adapter plug or wire please immediatel
27. ur sale department when changes SpO probe Chapter15 Maintenance and Cleaning A Warning AN Take cuff and the power source off before cleaning the unit or the SpO probe AN Caution AN E Do not subject the sensor to autoclaving E Do not immerse the SpO probe into any liquid E Do not use any SpO probe or cable that may be damaged or deteriorated Cleaning mM Use a cotton ball or a soft mull moistened with hospital grade ethanol to wipe the surface of the SpO probe and then dry it with a cloth This cleaning method can also be applied to the luminotron and receiving unit mM The cable can be cleaned with 3 hydrogen dioxide 70 isopropanol or other active reagent However connector of the SpO gt probe shall not be subjected to such solution Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Chapter16 Installation Of The Software 16 1 Demand Of Editor Pentium IV 1 8G or more Operation System Windows XP EMS memory 256M or more Hard Disk 40G or more Display 17 inch or more CD ROM USB 2 or more Resolution of printer 600 DPI 16 2 Installation Of Software 1 Place the CD ROM in the CD ROM compartment located on your computer 2 1 Auto Play for CDs is enabled place CD in reader and follow instructions when they appear in the screen otherwise follow install instructions below 1 Open Windows Explorer 2 Click on the root CD ROM directory 3 Double click file ContecO8A_Setup
28. y pulled the plug from the socket Otherwise it may cause electric shock or injury Do not plug or unplug the adapter power cord with wet hands Otherwise it may cause electric shock or injury Henrotech nv Acacialaan 8 2630 Aartselaar T 03 844 53 33 www henrotech be Operation for battery AN Note AN Please use 4 AA size manganese or alkaline batteries do not use batteries of other types Otherwise it may cause fire New and old batteries different kinds batteries can not be confusion Otherwise it may cause battery leakage heat rupture and damage to Electronic Sphygmomanometer and polarities of the batteries must match the polarities of the battery compartment as indicated When the batteries power exhausts replace with four new batteries at the same time Please take out the batteries when you do not use the device for a long time Otherwise it may cause battery leakage heat rupture and damage to Electronic Sphygmomanometer If battery fluid should get in your eyes immediately rinse with plenty of clean water Contact a physician immediately Otherwise it will cause blindness or other hazards If electrolyte of the batteries immodestly glues on the skin or the clothes immediately rinse with plenty of clean water Otherwise it may hurt the skin AN Advice AN Do not subject the device to strong shocks such as dropping the unit on the floor Do not inflate before the cuff wrapps around the arm Do not in
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