The VS2000 vital signs monitor is intended to be used in special procedure labs and other areas of a hospital or clinic where patient monitoring systems are needed. The standard parameters includes 5/3 leads electrocardiography(ECG), non-invasive blood pressure (NIBP), pulse oximetry (SpO2), Respiration Rate(RR), temperature(TEMP), optional parameter include ETCO2.
Main unit: 2 years
Accessories: 6 months
Technical Specification |
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Enclosure |
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Weight |
2.05 kg (4.52lbs) |
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Dimensions |
32.4cm × 12.9cm × 18.3cm |
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Display |
7.1-inch diagonal high-resolution TFT (Thin Film Transistor) Active Matrix LCD 800 X 480 |
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Alarms |
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Categories |
Patient status and system status |
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Notification |
Audible and visual |
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Setting |
Full storage, low battery and sensor off |
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Range |
Pulse rate (30-350bpm), SpO2 (0-100%), NIBP (0-300mmHg), RESP (5-150rpm), TEMP (24.5-45.5℃) |
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Alarm volume level |
45dBA to 85 dBA at 1 meter distance (adjustable) |
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Range, Accuracy and Resolution |
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Range Type |
Range Values |
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Measurement Ranges |
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SpO2 |
0-100% |
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Pulse rate |
30-350bpm |
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NIBP |
Systolic:40 to 270 mmHg Mean Arterial:30 to 220 mmHg Diastolic:20 to 200 mmHg |
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RESP |
0-150rpm |
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TEMP |
0-50℃ |
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Measurement Accuracy |
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SpO2 |
70-100% (±2%), <70% undefined |
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Pulse rate |
±2bpm/±2% take maximum |
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ETCO2 |
0~40mmHg ±2mmHg, 41~150mmHg ±10% |
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TEMP |
±0.2℃ |
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RESP |
±1rpm |
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Resolution |
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Display |
800 X 480 |
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SpO2 |
1% |
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ETCO2 |
0.1mmHg |
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TEMP |
0.1℃ |
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RESP |
1rpm |
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Pulse rate |
1bpm |
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Electrical |
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AC power requirement |
100-240VA, 50/60Hz |
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Power comsumption |
60VA,FUSE T1.5A |
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Batteries |
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Types |
Lithium-lon Batteries |
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Operating time |
≥4hours |
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Charge time |
≤4hours |
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Environment |
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Operating tempearture |
0-50℃ |
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Storage temperature |
-40-75℃ |
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Operating humidity |
15-95% |
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Storage humidity |
10-95% |
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Operating altitude |
-500-5000m |
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Standards and Certification |
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IEC 62366 |
Medical devices-Application of usability engineering to medical devices |
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IEC 62304 |
Medical device-software life cycle processes |
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MDD 93/42/EEC |
European Medical Device Directive |
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ISO 13485 |
Medical equipment-Quality management system |
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EN ISO 14971 |
Medical devices-Risk management |
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EN 60601-1 |
Medical electrical equipment |
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EN 60601-2 |
Medical electrical equipment |
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EN 60601-8 |
Medical electrical equipment |
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EN 980 |
Symbols for use in labeling of medical devices |
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EN 1041 |
Information supplied by the manufacture of medical devices |
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ISO 80601-2-61 |
Medical electrical equipment-Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
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EN ISO 10993-1 |
Biological evaluation of medical devices |
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EN ISO 10993-5 |
Biological evaluation of medical devices |
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EN ISO 10993-10 |
Biological evaluation of medical devices |
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ISO 14155-1 |
Clinical investigation of medical devices |
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CE |
CONFORMITE EUROPEENNE |
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SFDA |
State Food and Drug Administration |
Address:
20 Chapel Street,
Magill, SA 5072
Australia
ABN:22 630 524 935
Tel: 08 7073 9324
Email: info@utechmd.com.au