Inogen ONE G3 User Manual page 44

Inogen One® G3 Concentrator (continued)
Tested by Independent
Laboratory:
Classifications
Mode of Operation:
Type of Protection Against Electrical
Shock:
Degree of Protection to Concentrator
Components Against Electrical Shock:
Degree of Protection to Concentrator
Components Against Ingress of Water
While Used Outside of Carry Bag:
Degree of Protection to Concentrator
Components Against Ingress of Water
While Used Inside of Carry Bag:
Degree of Protection to Concentrator
Exterior Provided by the Carry Bag:
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.
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96-06947-00-01AG3 User Manual Inogen One G3HF-Multilanguage.indb 40
Safety: IEC 60601-1
CAN/CSA C22.2 No. 60601-1
Electromagnetic Compatibility:
IEC 60601-1-2
RTCA DO 160
Continuous Duty
Class II
Type BF
Not intended for cardiac application
IP20 - Not protected from dripping water.
Protected against ingress of solid
objects > 12.5 mm.
IP22 - Vertically dripping water shall have
no harmful effect & protect against
ingress of solid objects > 12.5 mm.
diameter when the enclosure is tilted
at an angle up to 15˚ from its normal
position
IP02 - Vertically dripping water shall have
no harmful effect when the enclosure
is tilted at an angle up to 15˚ from its
normal position
Not suitable for such application
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