Specifications; Devilbiss Guidance And Manufacturer's Declaration - DeVilbiss Healthcare SmartLink DV5M Série Manuel D'utilisation

Problem
Oximeter data
(SpO 2 and PR) not
displayed.
CPAP is not fully
functional.
dEVilBiSS SMaRtliNk SpEciFicatioNS
Size: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3.9" H x 3.1" W x 1.4" D (9.9cm H x 7.9cm W x 3.6cm D)
Weight: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0.30 lbs. (0.14 Kg)
Electrical Rating:
Maximum Power Consumption (SmartLink Module only): . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 W
Voltage and Current: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Power supplied by the DV5X Series Device
Class II Equipment; Type BF Applied Parts; Continuous Operation
Operating Conditions:
Temperature Range:. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41°F to 104°F (5°C to 40°C)
Humidity Range:. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 to 95% R.H. non-condensing
Atmospheric Conditions: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Sea level to 9,000' (2,743 M)
Transportation and Storage Conditions:
Temperature Range:. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .-40°F to 158°F (-40°C to +70°C)
Humidity Range:. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 0 to 95% R.H. non-condensing

dEVilBiSS guidaNcE aNd MaNuFactuRER'S dEclaRatioN

WaRNiNg
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and
put into service according to the Electromagnetic Compatibility [EMC] information provided in the
accompanying documents.
Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment.
The equipment or system should not be used adjacent to or stacked with other equipment and that if
adjacent or stacked use is necessary, the equipment or system should be observed to verify normal
operation in the configuration in which it will be used.
EN - 10
Probable Cause
1. Oximeter not properly
connected to the
SmartLink module.
2. Oximeter probe not
properly attached to user.
1. Module may be defective. 1. Remove the module from the CPAP and verify that
Remedy
1. Verify connection between the oximeter connector
and module oximeter connection port.
2. Reference the operating instructions that came with
oximeter.
CPAP is fully functional. If it functions properly
without the module connected, the module may be
defective. Contact provider. If it still is not fully
functional, consult the CPAP instruction guide for
troubleshooting.
A-DV5M-1