Philips IntelliVue CL SpO2 User Manual

10 Specifications
72
IntelliVue CL SpO2 Pod Specifications
Complies with ISO 9919:2005 / EN ISO 9919:2009.
Measurement Validation: The SpO
2
accuracy has been validated in human studies against arterial
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.
Physical Specifications
Size (W X H X D) 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)
Weight 80 g ±10%
2.8 oz ±10%
Robustness 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
Ingress Protection IP34 according to IEC 60529 (protection against ingress of water when
water drips, falls or splashes from any direction)
Environmental Specifications
Operating Temperature Range 0 to 40°C (32 to 104°F)
Operating Humidity Range ≤95% RH @ 40°C (104°F)
Operating Altitude Range -500 to 3000 m
Storage/Transportation Temperature
Range
-20 to 60°C (-4 to 140°F)
Storage/Transportation Humidity
Range
≤90% RH @ 60°C (140°F)
no condensation
Storage/Transportation Altitude Range -500 to 4600 m
Performance Specifications
SpO
2
Measurement Range 0 to 100%
Accuracy
The specified accuracy is the root-mean-square
(RMS) difference between the measured values
and the reference values
Mobile CL DSpO
2
-1A single patient sensor:
3% (70 to 100%)
Mobile CL RSpO
2
-1A reusable sensor:
3% (70 to 100%)
Resolution 1%
Pulse Oximeter Calibration Range 70% to 100%
Pulse

Philips IntelliVue CL SpO2 Specifications

General

Brand	Philips
Model	IntelliVue CL SpO2
Category	Measuring Instruments
Language	English