| SpO2 | |
| Saturation Normal (no motion): | 70-100%Arms ± 2% |
| Saturation Motion: | N/A |
| Low Perfusion: | N/A |
| Pulse Heart rate: | 20-300 BPM: ±3 BPM |
| Pulse Heart rate w/motion: | 20-300 BPM: ±3 BPM |
| | |
| Temperature | |
| Temperature Accuracy: | Quick Mode (Oral): ± 0.3°C |
| Temperature Accuracy: | Std. Mode (Aux/Rectal): ± 0.1°C |
| Temperature Accuracy: | Direct Mode ± 0.1°C |
| Response Time: | 4 sec (quick mode); 10-15 sec. (Axillary/Rectal); 60 sec.(direct mode) |
| Resolution: | 0.1°C |
| | |
| Blood Pressure | |
| Range: | Pressure: Diastolic: 20-200 mmHg (adult), 20-160 mmHg (pediatric). |
| | Systolic: 40-260 mmHg (adult), 40-230 mmHg (pediatric) |
| | Heart Rate: 30-220 BPM (beats per minute) |
| Accuracy (BP): | Meets or exceeds ANSI/AAMI/ISO 81060-2:2013 standard for non-invasive accuracy (±5mmHg mean error with 8mmHg standard deviation). |
| | |
| General Specifications | |
| Conditions for Use: | Operating: 10°C (50°F) to 40°C (104°F) 15 – 90% RH non-condensing - 700 kPa - 1060 kPa. |
| | Operating the monitor in an environment at maximum temperature can produce temperatures exceeding 41°C (41.6°C highest recorded) on a patient-applied part. |
| | It is up to the operator to determine if this temperature is too high based upon the condition of the patient and, if so, to ensure the ambient temperature of the environment is 38°C or below. |
| Storage: | -20°C (-4°F) to 55°C (149°F) 15 – 90% RH non-condensing - 500 kPa - 1060 kPa. Performance can be affected if used or stored outside the specified temperature, humidity, or altitude listed in the ranges above. |
| Power: | Internal power supply. Input: 100-240 VAC @ 1.5A max, 50-60 Hz. Output +9VDC @ 5A IEC 320 type input connector. |
| Battery: | Type: 7.2v, 6600mAh Internal Lithium-Ion battery Run Time (full charge): ~20 hrs* / 200 BP cycles Charge Time: ~6 hrs @ 23deg Celsius +/- 2deg |
| | *Unit with BP, Temp, SpO2, Wi-Fi, barcode scanner |
| Calibration: | The accuracy of cuff -pressure transducers/indicators should be verified bi-annually. |
| Safety Systems: | Independent hardware over-pressure circuit and redundant software overpressure algorithm to limit cuff pressure to less than 300 mmHg (+20/-10mmHg). Independent hardware timing circuit and redundant software timer algorithm to limit the duration of a blood pressure cycle to less than 180 seconds. |
| Dimensions: | Size (without thermometer option): 8” H x 6.75’’ W x 5.2’’ D or 215mm H x 190mm W x 140mm D |
| Standards: | ANSI/AAMI ES60601-1:2005/(R)2012 and A1:2012, C1:2009/(R)2012 and A2:2010/(R)2012, EN 60601-1:2006/A1:2013, IEC 60601-1-2: 2007 EMC, IEC 80601-2-30: 2013, ISO 80601-2-61: 2011, ISO 15223-1:2012, ISO 10993-1, 2009, ISO 10993-5, 2009, EN ISO 10993-10, 2010, ISO 81060-2:2013, EN 50419: 2006, EN ISO 14971:2009, CSA C22.2 No. 60601-1, EN ISO 81060-1: 2012, IEC 60601-1-6: 2013 |
| Classifications: | Equipment Classification: Class IIa per MDD, Class I (Electrical Shock), Continuous mode of operation, CE |
| Ingress of liquid: | Ingress Protection: IPX1: This device is protected against harmful effects of dripping water per IEC 60529. |
| | |
| Limited Warranty | |
| Main unit: | 3 years |
| SpO2 modules: | 4 years |
| Temp modules: | 5 years |
| Blood Pressure Cuffs: | 2 years |
| Battery: | 1 year |
| Accessories (SpO2 sensors, | 90 days |
| temp probes, BP hose, etc): | |
| | |
| Software | |
| ADView® 2 Driver for Windows - 32 bit | Download |
| ADView® 2 Driver for Windows - 64 bit | Download |