Intellivue Cl Spo2 Pod Specifications - Philips IntelliVue CL SpO2 Instructions For Use Manual

10 Specifications

IntelliVue CL SpO2 Pod Specifications

Complies with ISO 9919:2005 / EN ISO 9919:2009.
Physical Specifications
Size (W X H X D)
Weight
Robustness
Ingress Protection
Environmental Specifications
Operating Temperature Range
Operating Humidity Range
Operating Altitude Range
Storage/Transportation Temperature
Range
Storage/Transportation Humidity
Range
Storage/Transportation Altitude Range -500 to 4600 m
Measurement Validation: The SpO
blood sample reference measured with a CO-oximeter. Pulse oximeter measurements are statistically
distributed, only about two-thirds of the measurements can be expected to fall within the specified
accuracy compared to CO-oximeter measurements.
Display Update Period: Typical: 2 seconds, Maximum: 30 seconds. Maximum with NBP INOP
suppression on: 60 seconds.
Performance Specifications
SpO
2
Measurement Range
Accuracy
The specified accuracy is the root-mean-square
(RMS) difference between the measured values
and the reference values
Resolution
Pulse Oximeter Calibration Range
Pulse
72
53.5 mm x 27 mm x 65 mm ±5%
2.1 in x 1.1 in x 2.6 in ±5%
(without cradle and sensor)
80 g ±10%
2.8 oz ±10%
Provides essential performance during exposure to random vibration
according to IEC TR 60721-4-7 Class 7M1
Survives shock, random vibration and bump according to IEC TR
60721-4-7 Class 7M3 as well as a 1m drop
IP34 according to IEC 60529 (protection against ingress of water when
water drips, falls or splashes from any direction)
0 to 40°C (32 to 104°F)
≤95% RH @ 40°C (104°F)
-500 to 3000 m
-20 to 60°C (-4 to 140°F)
≤90% RH @ 60°C (140°F)
no condensation
accuracy has been validated in human studies against arterial
2
0 to 100%
Mobile CL DSpO -1A single patient sensor:
2
3% (70 to 100%)
Mobile CL RSpO -1A reusable sensor:
2
3% (70 to 100%)
1%
70% to 100%