Product Manual
Contents
1. C centigrade kHz kilohertz GHz Gigahertz Hz hertz kg kilogram m meter minute min minute mW milliwatt nm nanometer Symbols minus percent plus less than less than or equal to IA plus or minus copyright bpm beats per minute g gram MHz megahertz h hour K kilo kPa kilopascal M mega mm millimeters S second V volt negative per divide or equal to greater than gt greater than or equal x multiply 33 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL APPENDIX B Guidance and manufacturer s declaration electromagnetic immunity The Handheld Pulse Oximeter is intended for use in an electromagnetic environment specified below The customer or the user of the Pulse Oximeter should assure that it is used in such an environment Immunity IEC Compliance Test 60601 Level Electromagnetic environment Test level guidance Electrostatic 6kV 6kV Floors should be wood Discharge contact contact concrete or ceramic tile If floor ESD 8kV air 8kV air are converted with IEC610004 2 Synthetic material the relative humidity should be at least 3096 Guidance and manufacture s declaration Electromagnetic Immunity for Equipment and Systems that are not Life Supporting 35 d 80MHz to 800MHz 1 61000 4 6 23 800MHz to 2 5GHz 3V m Wher P is the maximum output power rating of the transmitter in Watts W according to the transmitt2. Always install or carry the equipment properly to avoid damage caused by drop impact strong vibration or other mechanical force NOTES Put the equipment in a location where you can easily see the screen and access the operating controls Keep this manual in the vicinity of the equipment so that it can be obtained conveniently when needed The software was developed in compliance with IEC60601 1 4 The possibility of hazards arising from Software errors is minimized SpO measurements may be influenced by high ambient light Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL especially sunlight Shield the sensor area if necessary Dyes introduced into the bloodstream such as methylene blue indocyanine green indigo carmine and fluorescein may influence the accuracy of the SpOz reading Any condition that restricts blood flow such as use of a blood pressure cuff or extremes in systemic vascular resistance may cause a failure to determine accurate pulse rate and SpOz readings Remove fingernail polish or artificial fingernails before applying SpO sensors Fingernail polish or artificial fingernails may cause inaccurate SpO readings Optical cross talk can occur when two or more sensors are located in adjoining areas It can be eliminated by covering each site with opaque material Optical cross talk may adversely affect the accuracy of the SpO readings Obstructions or dirt on the sen
3. Before use please verify whether the packages especially the packages of the single use accessories are intact In case of any damage do not apply it to the patient 3 2 Environmental Requirements The operating environment of the equipment must meet the requirements specified in this manual When the equipment is moved from one place to another condensation may occur as a result of temperature or humidity difference In this case never start the system before the condensation disappears Warning Make sure that the operating environment of the equipment meets the specific requirements Otherwise the equipment may not meet the specifications defined in this manual and unexpected consequences e g damage to the equipment may result 17 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL 3 3 Connect the sensor 1 Before use check the pulse oximeter for mechanical damage 2 Install the alkaline batteries and ensure that the batteries have sufficient power 3 Plug the SpO extension cable in the multifunctional connector on top of the oximeter as shown in figure 3 Ensure that the sensor is firmly plugged in FR f Fig 3 3 4 Starting or shutting off the oximeter To start the pulse oximeter 1 Press and hold the Power button for about 3 seconds The LED and alarm indicating lamp flashes and then goes out The system gives a beep and displays the startup screen The startup screen displays the ver
4. anemia or hypothermia d An arterial occlusion proximal to the sensor AN WARNINGS Use only SpO sensors provided by manufacturer Other SpO sensors may cause improper performance Do not use SpO sensor with exposed optical components Excessive patient movement may cause inaccurate measurements Tissue damage can be caused by incorrect operation or misusing sensor for example by wrapping the sensor too tight Inspect the sensor site to ensure the skin s integrity and the adhesion position of the sensor is correct More frequent inspection should be taken if necessary Loss of pulse signal can occur in any of the following situations a The sensor is too tight b There is excessive illumination from light sources 22 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Such as a surgical lamp a bilirubin lamp or sunlight C A blood pressure cuff is inflated on the same extremity as the one to which an SpO sensor is attached NOTES Pulse sensor should obviate the light source e g radial lamp or infrared lamp 5 VISUAL ALARM INDICATORS If an alarm threshold is exceeded the corresponding data area will flash If the alarm is activated by more than one physiological alarm each parameter will flash 5 1 AUDIBLE ALARM INDICATORS Audible alarms can be heard provided the mute features is not engaged The audible alarm has different tone pitch and on off beep patterns for each alarm
5. i 3 Medical Silicon neonates when used with this device ABS Medical clip sensor Silicon Soft fingertip sensor Medical Silicon Soft fingertip sensor Medical Silicon ucueral Descriptions The handheld pulse oximeter adapts 8 segment digital LED for displaying data It can display the SpO and pulse rate value pulse bar as well as battery status etc 2 1 Front panel Please refer to Fig 1 The display in fig 1 is normal screen 11 oximeter Series PULSE OXIMETER INSTRUCTION MANUAL al Fig1 Front panel Instruction of figure 1 1 SpO2 value 2 PR Pulse rate 3 Low power indicator When the power is lower than 2 4V the lamp indicated by it will be lighted And the oximeter will 12 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL power off automatically when the power is lower than 2 3V 4 Alarm Indicator When technical alarm or physiological alarm occurs the lamp indicated by it will turn red 5 Power button Pulse bar The pulse bar is in proportion to the Pulse volume Note This manual describes all features and options Your equipment may not have all of them 2 2 Rear panel 13 lloximeter Series PULSE OXIMETER INSTRUCTION MANUAL Fig 2 Rear panel Rear panel introduction 1 Batteries 2 Fixing hole 3 Fixing screw 4 Battery Wharf cover Batteries Installation 1 Open the battery cover Rotate the fixing screw sli
6. priority High priority SpO alarm beeps every 8 seconds Medium priority PR alarm beeps every 8 seconds Low priority Sensor off or finger out beeps every 20 seconds 23 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL 5 2 ALARM ACTIVATION Alarm will be activated on following conditions Physiological alarm Technical alarm error code a Error Definitions E 1 program memory is damaged E 3 Signal strength is too weak to be detected E 4 Sensor is unplugged E 5 No finger is inserted or sensor goes wrong E 6 The oximeter can not search for pulse E 7 It takes too long to search pulse E 8 Pulse alarm is malfunctioning E 9 The SpO value is lower than the low limit E 10 The SpO value is higher than the high limit E 11 The value of pulse rate is lower than the low limit E 12 The value of pulse rate is higher than the high limit E 13 Power supply is insufficient When the E9 E10 E11 or E12 occurs the value of parameter will flash Check the error code Press the right arrow key under normal screen it will indicate any existing error codes To return to normal 24 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Screen please press menu button again A Warnings When alarm occurs Check which type of alarm is issued e Check patient s condition if parameter alarm is issued Make the alarm mute if necessary Check whether the alarm is in proper condition case of no warni
7. rate displayed value is 67 bpm now 2 5 Factors that may affect the measurement During operation the accuracy of oximetry readings can be affected by the following factors 2 5 4 Instrument performance depends the pulsatile character of the artery The measurement would not be 20 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL considered reliable and accurate if the following conditions are present during measurement Shock or cardiac arrest Extreme temperature of the digit After the administration of a cardiovascular drug Anemia Evidence of ventilation perfusion mismatch 2 5 2 Instrument performance depends on the wavelength absorption for oxyhemoglobin and deoxyhemoglobin If there are substances absorbing the same wavelength this would induce false or low 5 values The following may affect these values carboxyhemoglobin methemoglobin methylene blue Indigo carmine 2 5 8 Extremely high illumination could affect the SpO measurement Use a semi translucent or opaque cover to shield the sensor 2 5 4 Other factors a High frequency electrosurgical interference from external devices including defibrillators 21 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL b Placement of a sensor on an extremity that currently has installed a blood pressure cuff arterial catheter or intravascular line c The patient has hypotension severe vasoconstriction severe
8. the patient s condition may require changing the sensor site periodically Change the sensor site and check skin integrity circulatory status and correct alignment at least every 4 hours Prolonged use may cause blisters skin deterioration and discomfort When connecting this oximeter to any instrument verify proper operation before clinical use Refer to the instrument s user manual for full instructions The equipment connected to the pulse oximeters data interface must be certified according to the respective IEC standards i e IEC950 for data processing equipment or IEC 601 1 for medical electrical equipment All combinations of equipment must be in compliance with IEC601 1 1 systems requirements Sensor malfunction may cause inaccurate data possibly resulting in patient injury or death so pay close attention to the sensor and inspect it often The physiological data and alarm messages displayed on the equipment are for reference only and cannot be directly used 4 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL for diagnostic interpretation Do not rely exclusively on the audible alarm system for patient monitoring Adjustment of alarm volume to off may result in a hazard to the patient Remember that alarm settings should be customized according to different patient situations and always keeping the patient under close surveillance is the most reliable way for safe patient monitoring Worn out data c
9. work shall be done at Drive s standard rates and charges in effect at the time of delivery to Drive APPENDIX A Specifications Display Data SpO2 PR Others connection status of probe and other alarm information Alarm Alarm SpO2 and pulse rate value probe off battery exhausted Alarm mode audio alarm visual alarm and error code 31 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Alarm limits range 70 100 Default limits High 99 low 90 SpO Display range 0 100 Measurement range 70 100 Resolution 1 Accuracy 3 70 100 Unspecified 0 69 Measurement Wavelengths and Output Power Red 660nm 3mw nominal Infrared 940nm 3mw nominal Pulse Rate Display range 0 254bpm Measurement range 30 235bpm Resolution 1bpm Accuracy 30 99bpm 2 100 235 2 Operation Environment Operating temperature 5 G 40 C Relative humidity lt RH80 no condensation Atmosphere pressure 86kPa 106kPa Power supply Two AA alkaline batteries Working time work for 30 hours continuously Abbreviations CISPR International Special Committee on Radio Interference EEC European Economic Community EMC Electromagnetic Compatibility 32 Oximeter Series MANUAL ID Identification PULSE OXIMETER INSTRUCTION IEC International Electrotechnical Commission LED Light Emitting Diode PR Pulse Rate RF Radio Frequency SpO Arterial Oxygen Saturation from Pulse Oximeter Abbreviations A ampere
10. 4 0946 Fax 516 998 4601 36
11. HANDY OX HAND HELD PULSE OXIMETER INSTRUCTION MANUAL Model 18715 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Contents TIntrod ctioni 52 a E 3 1 1 Brief Introduction 3 1 2 Safety 3 1 3 Equipment symbols 8 1 4 Electromagnetism 9 1 5 Equipment 9 1 6 ooo ERREUR RR RR d ee 10 2 General Descriptions 15522 11 2 1 Front panel 2 2 eee 11 2 2 Rear 13 2 3 5 aene 16 2 4 Product TEAU OS ooo o a e aw vg 16 2 5 Intended 16 3 Getling Started 16 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL 4 19 5 Maintain 25 51 26 5 2 Calibration and Verification 28 5 3 Warranty iiissssssceeeeeeeeeee sese a 27 APPENDIX A 30 APPENDIX B eoo RURSUM NUR NR M 34 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL 1 Introduction 1 1 Brief Introduction Thank you for pur
12. ables may also cause inaccurate data so if the data is used as a reference to treat a patient pay special attention to data cable and check it more frequently When using the equipment with electrosurgical units ESU make sure the patient is safe Do not come into contact with the patient during defibrillation Otherwise serious injury or death could result Single use accessories should never be reused To avoid inadvertent disconnection route all cables in a way to prevent a stumbling hazard Wrap and secure excess cabling to avoid risk of entanglement or strangulation by patients or personnel CAUTIONS Autoclaving ethylene oxide sterilizing or immersing the sensors in liquid may cause inaccurate readings To ensure patient safety use only parts and accessories specified in this manual Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL The operator must be thoroughly familiar with the information in this manual before using the device Unplug the sensor from the oximeter before cleaning or disinfecting it f liquid is accidentally spilled on the unit clean and dry thoroughly before reuse Do not try to use the SpO2 and NIBP measurement on the same arm at the same time This could potentially affect measurement accuracy At the end of its service life the equipment as well as its accessories must be disposed of in compliance with the guidelines regulating the disposal of such products
13. chasing this handheld pulse oximeter The device is designed to measure oxygen saturation SpO and Pulse Rate PR delivering visual and audio alarm Please read this manual carefully before using it 1 2 Safety Information Concepts of Warning Caution and Notice The Warning Caution and Notice labels in this document are intended to facilitate safe user operation of this product Warning Indicates a potential hazard or unsafe practice that if not avoided will result in death or serious injury Caution Indicates a potential hazard or unsafe practice that if not avoided could result in minor personal injury or product property damage Notice Provides application tips or other useful information to ensure that you get the most from your product WARNINGS Before putting the system into operation verify that the equipment connecting cables and accessories are in correct working order and operating condition Do not use the oximeter in the presence of flammable anesthetics vapors or liquids Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Do not use the oximeter in an MRI or CT environment Do not open the equipment housings electric shock hazard may exist All servicing and future upgrades must be carried out by the personnel trained and authorized by our company only The pulse oximeter is specified for use by medical professionals only Prolonged use of the probe sensor or
14. due to close proximity or strength of a source may result in disruption of performance of this device This apparatus complies with the IEC 60601 1 2 international standard The requirements of this international standard are CISPR11 GROP1 and CLASS B 1 5 Equipment classification Classification according to IEC 60601 According to the type of Internal electrical power protection against source equipment Electrical shock According to the degree of Type B equipment protection against Oximeter Series MANUAL Electrical shock PULSE OXIMETER INSTRUCTION According to the degree of protection against harmful ingress of water Ordinary equipment enclosed equipment without protection against ingress of water According to the methods of sterilization or disinfection Non sterilizable Use of Liquid surface disinfectants only According to the mode of operation continuous operation Equipment not suitable for use in the presence of a flammable anesthetic mixture air or with oxygen or nitrous oxide 1 6 Accessory Standard accessories 1 2 3 4 Specification for SpO Sensor Two AA Size Alkaline batteries Operator s manual One finger sensor One bind 10 loximeter Series PULSE OXIMETER INSTRUCTION MANUAL Sort Materials ABS Medical clip sensor Silicon ABS Medical clip sensor Km Silicon binding sensor is not intended for use in
15. er manufacture and d is the recommended Radiated 80Hz separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site RF IEC to 2 5 GHz survey should be less than the compliance level in each frequency range Interference may occur in the vicinity of 61000 4 3 equipment marked with the following symbol NOTE1 At 80MHz and 800MHz the higher frequency range applies NOTE2 These guideline may not apply in all situations Electromagnetic propagation is affected 34 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL by absorption and reflection from structures objects and people Field strengths from fixed transmitters such as base situation 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 Handheld Pulse Oximeter is used exceeds the applicable RF compliance level above the Handheld Pulse Oximeter should be observed Recommended separation distances between portable and mobile RF communications equipment and the handheld Oximeter The handheld Oximeter is intended for use in an electromagnetic environment in which radiated RF disturbance are con
16. ghtly in the rear panel to the up position which is marked with and then open the cover 2 Install 2 batteries lightly as indicated by the polarity sign Note Be sure to insert the batteries in the correct polarity as indicated by polarity markings and inside the battery wharf 14 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL 3 Close battery cover Close the battery cover and rotate the screw to the position And the batteries are locked A Make sure that the polarity of the batteries is correct Otherwise the unit cannot operate normally Battery life and replacement When the low power indication lamp is lighted please replace the batteries with new ones timely Always turn the unit off before replacing the batteries lt Dispose of the used batteries according to the applicable local regulations A Warnings If battery fluid should get into your eyes immediately rinse with plenty of clean water Consult a doctor immediately Cautions Do not use batteries not specified for this unit Do not insert the batteries with the polarities in the wrong direction lt Do not dispose of batteries in fire If battery fluid should get on your skin or clothing immediately rinse with plenty of clean water Remove the batteries from this unit when you are not going to use it for a long period of time approximately three months or 15 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL m
17. nfection may cause damage to the equipment and is therefore not recommended for this pulse oximeter CAUTION Never use EtO or formaldehyde for disinfection 9 2 Calibration and Verification The performance should be checked every one year and after maintenance and repair Required Test Equipment SpO signal Simulator Notice The simulator cannot be used to assess the accuracy of a pulse oximeter probe or a pulse oximeter 9 2 SpO amp Pulse Rate Measurement Value Verification 28 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL a Connect SpO Probe to the SpO connector on the oximeter b Insert the operators finger into the finger sensor the SpOs measured value of healthy person should be from 95 to 100 and the pulse rate is same as heart rate If 5 Simulator is available verify the accuracy of Oxygen Saturation Value with probes as follows Tolerance 2 2 3 Oxygen Saturation 96 86 70 9 2 4 5 amp Pulse Rate Alarm Verification a Connect SpO Probe to the 5 connector on the oximeter b Insert the operators finger into the finger sensor the SpOs measured value of healthy person should be more than 95 Set the SpO high limit as 90 low limit as 80 d Verify the SpOs visual and auditory alarms the background color of the 5 data should be red and beep sound should be heard 9 3 Trouble Shooting a Can t power on the oximeter Please check
18. ng 8 Beep on off Press the menu key five times under the normal screen to enter access to this function associated screen will be displayed Press up or down key to set the pulse beep on off 9 Maintain and Cleaning Use only the substances approved in this manual and methods listed in this chapter to clean or disinfect your equipment Warranty does not cover damage caused by unapproved substances or methods We make no claims regarding the efficacy of the listed chemicals or methods as a means for controlling infection For the method to control infection consult your hospital s Infection 25 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Control Officer or Epidemiologist Keep your equipment and accessories free of dust and dirt To avoid damage to the equipment follow these rules Always dilute according the manufacturer s instructions or use lowest possible concentration Do not immerse part of the equipment into liquid Do not pour liquid onto the equipment or accessories Do not allow liquid to enter the case Never use abrasive materials such as steel wool or silver polish or erosive cleaners such as acetone or acetone based cleaners 9 1 Safety Checks Before every use or after your pulse oximeter has been used for 6 to 12 months or whenever your pulse oximeter is repaired or upgraded a thorough inspection should be performed by qualified service personnel Follow these guidelines when inspecting
19. ore Do not use batteries of a different type together lt Do not use new and used batteries together 2 3 Right side panel A band delivered together with the oximeter can be inserted into the 8 shape hole on the right side of the oximeter The band can help with continuous operation 2 4 Product features lt Rubber grip design offers special protection lt Compact light weight design for simple one hand operation lt High brightness LED displays SpO pulse rate and pulse bar Visual amp audio alarm low battery alarm lt Convenient 2 AA size alkaline batteries 2 5 Intended use The handheld pulse oximeter is intended for continuous monitoring spot checking of functional pulse oxygen saturation 96SpO and pulse rate PR of single adult pediatric patients in hospitals and home care 3 Getting started 3 1 Unpacking and Checking Before unpacking examine the packing case carefully for damage If any damage is detected contact the carrier If the 16 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL packing case is intact open the package and remove the equipment and accessories carefully Check all materials as per the packing list and check for any mechanical damage WARNINGS Keepthe packing material out of children s reach Disposal of the packaging material should observe the applicable waste control regulations The equipment might be contaminated during storage and transport
20. sion no of software 2 The startup screen disappears and the pulse oximeter enters the 18 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL normal screen To shut off the pulse oximeter 1 Confirm that the patient measurement is finished 2 Disconnect the SpO extension cable from the pulse oximeter 3 Press and hold the Power button for 4 seconds WARNING Do not use the pulse oximeter if you suspect it is not working properly or if it is mechanically damaged Contact the carrier or our service department immediately 5 Take a measurement SpO measuring is a non invasive technique used to measure the amount of oxygenated hemoglobin and pulse rate by measuring the absorption of selected wavelengths of light The light emitted by a red and infrared light emitting diodes passes through the tissue and is converted into electrical signals by a photodiode 19 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL Fig 6 placement of the sensor e Select the suitable sensor in terms of type and dimension e Clip the sensor to the patient s finger as shown above And ensure that the patient s nail surface is facing upward Plug sensor into SpO port on top panel of pulse oximeter Note To maintain the highest degree of accuracy it is recommended that the finger and the oximeter sensor probe are kept as still as possible Description of Fig 7 SpO2 value displayed value is 98 now PR Pulse
21. sor s red light or detector may cause a sensor failure Make sure there are no obstructions and the sensor is clean For routine equipment maintenance please refer to the Service procedures at the associated section as indicated in the manual As to the other concerns for attention please carefully look through the specific chapter in this instruction Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL This manual describes all features and options Your equipment may not have all of them Federal Law restricts this device to sale by or on the order of a physician 1 3 Equipment symbols Symbol AN Definitions Attention Read the operator s manual carefully before using the oximeter Type BF applied part Production date Manufacturer s address ud Low power indicator CE European union approval Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL sn Serial number 1 4 Electromagnetism interference This oximeter is designed and tested in compliance with the EMC standard complying with the international standard for the EMC of the electronic medical device IEC 60601 1 2 However because of the proliferation of radio frequency transmitting equipment and other sources of electrical noise in the health care and home environments e g cellular phones mobile two way radios electrical appliances it is possible that high levels of such interference
22. the batteries voltage 29 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL b SEn oFF alarm Please check if the probe was connected with the oximeter correctly or the finger is inserted fully If the sensor is with extension cable please check if the extension cable is connected with the sensor correctly C E1 E2 E8 E14 alarm Please contact our service department d ES E6 E7 alarm Check the patient condition and other please contact our Service department Warranty Drive warrants to the purchaser for 2 years from the date of purchase each oximeter exclusive of the battery Drive will repair or replace any oximeter found to be defective in accordance with this warranty free of charge for which Drive has been notified by the purchaser by serial number that there is a defect provided notification occurs within the applicable warranty period 30 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL This warranty excludes cost of delivery to and from Drive Drive reserves the right to charge a fee for a warranty repair request on any oximeter found to be within specifications The Drive handheld pulse oximeter is a precision electronic instrument and must be repaired by Drive Technical Support Any sign or evidence of opening the oximeter field service by non Drive personnel tampering or any kind of misuse of the oximeter shall void the warranty The oximeter is warranted for consumer use only All non warranty
23. the equipment Make sure that the environment and power supply meet the requirements e Inspect the equipment and its accessories for mechanical 26 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL damage Make sure that only specified accessories are applied Inspect if the alarm system functions correctly Make sure that the batteries meet the performance requirements e Make sure that the pulse oximeter is in good working condition In case of any damage or abnormity do not use the pulse oximeter Cleaning Your equipment should be cleaned on a regular basis If the unit is dirty the equipment should be cleaned more frequently Before cleaning the equipment consult your hospital s regulations for cleaning the equipment Recommended cleaning agents are Mild soap diluted Ammonia diluted Sodium hypochlorite bleach diluted Hydrogen peroxide 396 Ethanol 7096 Isopropanol 7096 To clean your equipment follow these rules 1 Shut down the pulse oximeter and take the batteries out of the battery wharf 27 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL 2 Clean the display screen using a soft clean cloth dampened with a glass cleaner 3 Clean the exterior surface of the equipment using a soft cloth dampened with the cleaner 4 Wipe off all the cleaning solution with a dry cloth after cleaning if necessary 5 Dry your equipment in a ventilated place Disinfecting Disi
24. trolled The customer or the user of the handheld Pulse Oximeter can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communication equipment transmitters and the oximeter as recommended below according to the maximum output power of the communications equipment Rated Separation distance according to frequency of transmitter m maximu m output 150KHz to 80 MHz 80MHz to 800 800MHz to 2 5 GHz power of ge 33A MHz transm V itter 3 5 W E 0 01 0 1167 0 1167 0 2334 0 1 0 3689 0 3689 0 7378 1 1 1667 1 1667 2 3334 10 3 6893 3 6893 7 3786 100 11 6667 11 6667 23 3334 For transmitters rated at a maximum output power not listed above the recommended separation distance in meters 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 35 Oximeter Series PULSE OXIMETER INSTRUCTION MANUAL NOTE1 At 80MHz and 800MHz the separation distance for the higher frequency range applies NOTE2 These guidelines may not apply in all situations Electromagnetic interference is affected by absorption and reflection from structures objects and people DRIVE MEDICAL 99 Seaview Blvd Port Washington NY 11050 www drivemedical com Phone 516 998 4600 Toll Free 877 22
Download Pdf Manuals
Related Search