Inogen One G2 Manuel D'utilisation page 22

Inogen One® G2 Concentrator (continued)
Tested by Independent Safety: IEC 60601-1
Laboratory: CAN/CSA C22.2 No. 60601-1
Electromagnetic Compatibility:
IEC 60601-1-2
RTCA DO 160
Classifications
Mode of Operation:
Type of Protection Against Electrical
Shock:
Degree of Protection Against Electrical
Shock:
Degree of Protection Against Ingress of
Water:
Degree of Safety for Application in
Presence of Anesthetic Gases:
ELECTrOMAGNETIC COMPATIBILITy
This CE Marked equipment has been tested and found to comply with the EMC limits for
the Medical Device Directive 93/42/EEC [EN 55011 Class B and EN 60601-1-2]. These limits
are designed to provide reasonable protection against harmful interference in a typical
medical installation.
The equipment generates uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause harmful interference
to other devices in the vicinity.
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Continuous Duty
Class II
Type BF
Not intended for cardiac application
IP20
Not suitable for such application
However, there is no guarantee that interference will not occur in a particular installation.
If this equipment does cause harmful interference with other devices, which can be
determined by turning the equipment off and on, the user is encouraged to try to correct
the interference by one or more of the following measures:
1. Reorient or relocate the receiving device.
2. Increase the separation between the equipment.
3. Connect the equipment into an outlet on a circuit different from that to
which the other device(s) is connected.
4. Consult Inogen or your equipment provider for assistance.
CAUTION Portable and mobile RF communications equipment can affect medical
electrical equipment.
CAUTION Stacking or placing equipment adjacent to other devices is not
recommended, where such configurations are necessary, all equipment
in question should be carefully observed to ensure that EMI does not
degrade performance.
CAUTION Use of accessories, transducers, and cables other than those specified,
with the exception of transducers and cables sold by the manufacturer
of the equipment as replacement parts for internal components,
may result in increased emissions and decreased immunity of the
equipment or system.
Inogen One® G2 System Specifications Chapter 8
39