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Certification 

This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing specifications when it 

was shipped from the factory. Calibration measurements are traceable to the National Institute of Standards and Technology (NIST). 

Devices for which there are no NIST calibration standards are measured against in-house performance standards using accepted 

test procedures. 

WARNING 

Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards or 

improper operation. Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment modifications. 

Restrictions and Liabilities 

Information in this document is subject to change and does not represent a commitment by Fluke Biomedical. Changes made to the 

information in this document will be incorporated in new editions of the publication. No responsibility is assumed by Fluke Biomedical 

for the use or reliability of software or equipment that is not supplied by Fluke Biomedical, or by its affiliated dealers. 

Manufacturing Location 

The ProSim™ 8 Vital Signs Simulator is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A. 

 

Содержание 3979409

Страница 1: ...uary 2011 Rev 3 3 16 2011 2016 Fluke Corporation All rights reserved Specifications are subject to change without notice All product names are trademarks of their respective companies ProSim 8 Vital S...

Страница 2: ...ke Biomedical service facility NO OTHER WARRANTIES SUCH AS FITNESS FOR A PARTICULAR PURPOSE ARE EXPRESSED OR IMPLIED FLUKE SHALL NOT BE LIABLE FOR ANY SPECIAL INDIRECT INCIDENTAL OR CONSEQUENTIAL DAMA...

Страница 3: ...sk for an agent to be present while the instrument is unpacked There are no special unpacking instructions but be careful not to damage the instrument when unpacking it Inspect the instrument for phys...

Страница 4: ...ct all instrument surfaces Use nonabrasive material around all projecting parts Use at least four inches of tightly packed industry approved shock absorbent material around the instrument Returns for...

Страница 5: ...esult in electrical shock hazards or improper operation Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment modifications Restrictions and Liabilities Inf...

Страница 6: ......

Страница 7: ...that the electronics within the pulse oximeter probe are functional The intended user is a trained biomedical equipment technician who performs periodic preventative maintenance checks on patient mon...

Страница 8: ...before you use the Product Do not touch voltages 30 V ac rms 42 V ac peak or 60 V dc Do not use the Product around explosive gas vapor or in damp or wet environments Examine the case before you use t...

Страница 9: ...duct Use only the mains power cord and connector approved for the voltage and plug configuration in your country and rated for the Product Replace the mains power cord if the insulation is damaged or...

Страница 10: ...ry packs near heat or fire Do not put in sunlight Do not short the battery terminals together Do not keep cells or batteries in a container where the terminals can be shorted Remove the input signals...

Страница 11: ...uirements of the U S Federal Communications Commission Conforms to relevant South Korean EMC Standards Spent Lithium batteries should be disposed of by a qualified recycler or hazardous materials hand...

Страница 12: ...6 Instrument Familiarization Table 2 is a list of Product top panel controls and connections shown in Figure 1 F1 F2 F3 F4 F5 Top 14 13 10 11 9 8 7 6 5 4 2 3 15 16 18 17 1 12 glh034 eps Figure 1 Top...

Страница 13: ...al Functions Accesses the temperature respiration cardiac output fetal simulation autosequences and view memory functions SETUP Button Accesses the setup controls IBP Button Accesses the Invasive Bloo...

Страница 14: ...tor Connector to the SpO2 accessory IBP Channel 2 Connector Connector to an IBP input of the patient monitor Cardiac Output Connector Connector to the Cardiac input of the patient monitor IBP Channel...

Страница 15: ...igns Simulator Instrument Familiarization 9 Table 3 is a list of Product controls and connections shown in Figure 2 Front Right Back 1 4 7 8 5 6 2 3 glh035 eps Figure 2 Back Front and Side Panel Conne...

Страница 16: ...y Latch Locks the battery pack into the Product Push down to remove the battery pack Mini B USB Device Port Used to connect to a PC for remote control or download test results data to a PC USB A Contr...

Страница 17: ...to use See the Users Manual for detailed instructions General Specifications Temperature Operating 10 C to 40 C 50 F to 104 F Storage 20 C to 60 C 4 F to 140 F Humidity 10 to 90 non condensing Altitu...

Страница 18: ...internal function of the equipment itself Class A Equipment is suitable for use in all establishments other than domestic and those directly connected to a low voltage power supply network that suppl...

Страница 19: ...ecifications Normal Sinus Rhythm Waveform ECG Reference The ECG amplitudes specified are for Lead II calibration from the baseline to the peak of the R wave All other leads are proportional Normal Sin...

Страница 20: ...elevation of 0 mV Pacemaker Waveform Pacer Pulse Amplitude 0 mV off 2 mV 4 mV 6 mV 8 mV 10 mV 12 mV 14 mV 16 mV 18 mV 20 mV 50 mV 100 mV 200 mV 500 mV and 700 mV for lead II reference lead Accuracy R...

Страница 21: ...Arrhythmia PVCs 6 per minute 12 per minute or 24 per minute frequent multifocal PVCs bigeminy trigeminy multiple PVCs one time run of 2 PVCs 5 PVCs or 11 PVCs mono ventricular tachycardia 120 BPM to 3...

Страница 22: ...onomorphic ventricular tachycardia 120 BPM to 300 BPM Torsade De Pointes Polymorphic ventricular tachycardia long QT interval ECG Performance Testing Amplitude peak to peak 0 05 mV to 0 5 mV 0 05 mV s...

Страница 23: ...teps and 20 ms to 200 ms in 10 ms steps Width Accuracy 1 of setting 1 ms Rate 30 BPM 60 BPM 80 BPM 120 BPM 200 BPM and 250 BPM R Wave up slope 0 875 amplitude 0 4375 x width R Wave down slope Full amp...

Страница 24: ...d pressure curve from 0 mmHg to 90 mmHg and returning to 0 mmHg IUP Period 2 minutes 3 minutes or 5 minutes and manual Default Settings FHR 140 BPM early deceleration wave manual Invasive Blood Pressu...

Страница 25: ...t atrium right ventrical RV pulmonary artery PA pulmonary artery wedge PAW Cardiac Catheterization Chambers Aortic Pulmonary valve and Mitral valve Respiration Artifact Arterial radial artery and left...

Страница 26: ...0 Output Circular DIN 4 pin Cardiac Output Catheter Type Baxter Edwards 93a 131 7f Calibration Coefficient 0 542 0 C injectate 0 595 24 C injectate Blood Temperature 36 C 98 6 F to 38 C 100 4 F 0 2 C...

Страница 27: ...c MAP Adult 60 30 40 80 50 60 100 65 77 120 80 93 150 100 117 and 200 150 167 and 255 195 215 Neonatal 35 15 22 60 30 40 80 50 60 100 65 77 120 80 93 and 150 100 117 Pressure variability Systolic and...

Страница 28: ...1 Accuracy With oximeter manufacturer s R curve Saturation within UUT specific range 1 count specified accuracy of the UUT Saturation outside UUT specific range monotonic with unspecified accuracy Wi...

Страница 29: ...on 0 01 Artifact Respiration Range 0 to 5 of transmission Resolution 1 Rate all ProSim respiration simulation settings Ambient Light Range 0X to 5X transmitted light Resolution 1X Frequency DC 50 Hz 6...

Страница 30: ...rdic Bradycardic Ventricular Fibrillation Asystole Autosequences default Monitor testing sequence Medical training sequence Oximeter testing sequence Cardiac failure sequence Arrhythmia sequence Exerc...

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