| Measurement Range | - Saturation (SpO2): 1 - 100%
- Pulse rate (PR): 0 - 300 BPM
- Perfusion index (PI): 0.1 - 20 CO2
|
| Accuracy | - Saturation +/- 2% (70 - 100%, without motion artifacts)
- Pulse frequency +/- 3 BPM (30 - 250 BPM, without motion artifacts) 0%, 1-2%, >5%
|
| Display | - Data update rate: once every 300 ms
- Plethysmogram: amplitude = 75% of the measuring range
|
| Operating Temperature | 0°C - 40°C (32°F - 104°F) |
| Operating Humidity | 15 - 95% relative humidity (non-condensing) |
| Ambient Pressure | 700 - 1060 hPa |
| Storage Temperature | -25°C - 70°C (-13°F - 158°F) |
| Battery | Li-ion 3.6 V 2900 mAh |
| Operating Time Per Charge | - > 18 hours (at standard settings),
- > 24 hours (when auto-off function is switched on and at lowest brightness setting for display)
|
| Charger | - Mini-USB Type B, Protection Class II, Input: AC 110 V - 230 V / 50 - 60 Hz / 125 mA, Output: DC 5 V / min. 1 A / < 15 W, IEC 60601-1 / IEC 60950-1
|
| Charge Time | Approx. 4 hours (full functionality maintained while charging) |
| Display | 2.8" multicolor TFT |
| Dimensions (Device) | 160 x 72 x 39 mm / 6-1/4 x 2-3/4 x 1-1/2 inch (H x W x D) |
| Protection Class | IP 54 |
| Impact Resistance | IK 05 |
| Weight | Approx. 320 g (with sensor) |
| Interface | USB 2.0 (Mini-USB Type B connector) |
| Alarm Functions | Monitoring of alarm limits and device functions (optical and acoustic) |
| Alarm Limits (Adjustable) | - SpO2 - Upper limit: 51% - 100% SpO2, Lower limit: 50% - 99% SpO2
- Pulse - Upper limit: 31 - 250 BPM, Lower limit: 30 - 249 BPM
|
| Alarm Volume | 55 - 75 dB(A) |
| Pulse Tone | Tone pitch variable (depending on measured SpO2 value) |
| Application Indicator | Period 0 - 8 hours |
| Data Storage | Max. 96 hours at a trend storage interval of 10 seconds (trend storage interval adjust able from 5 - 60 seconds) readings, date, time, alarm limits, events |
| Personalization | Device and data set in connection with MySign software (e.g. name, ward, patient ID) |
| Electrical Safety | Class II, Type BF |
| MDD Class | IIb |
| Conformity | CE 0123 |
| Standards | The device complies with the requirements of MDD 93/42/EEC for medical devices and the applicable standards (e.g. ISO 80601-2-61) and directives. Also in compliance with: DIN EN 1789 medical vehicles and their equipment - road ambulances |
