Inogen Rove 6 Manuel D'utilisation page 51

17. SYMBOLS
U.S. Federal Regulation Restricts this Device to Sale
by order of Physician.
May also be applicable in other Countries
Type BF Applied Part
Class II Equipment
No Open Flames (Concentrator); Do not incinerate
(Battery).
No smoking
No oil or grease
Importer
Electrical Safety Agency Certificate
European Conformity
The manufacturer of this POC has determined this
device conforms to all applicable FAA requirements
for POC carriage and use on board aircraft.
Medical device
Protected from touch by fingers and objects greater
than 0.5 in (12.5 mm).
Protected from dripping water less than
15 degrees from vertical.
Indicates the range of humidity to which the medical
device can be safely exposed
Warning or caution. Attention required.
Packaging is recyclable
Compliant with the Waste Electrical and Electronic
Equipment/Restriction of the Use of Certain
Hazardous Substances in Electrical and Electronic
Equipment (WEEE/RoHS) recycling directive.
Date of Manufacture
Contents
CH Authorized Representative
CH REP
©2022 Inogen, Inc. All rights reserved.
Keep Dry
Indoor or Dry Location Use Only,
Do Not Get Wet
AC Power
DC Power
Refer to instruction manual/booklet
Manufacturer
Authorized Representative in the European
Community/European Union
Indicates use of the automobile DC power cord
(BA-306)
Indicates not for use in MRI environment
The Federal Communications Commission
Unique Device Identification
Serial Number
Patient information website
Some information for use are available on the web
Catalog Number
United Kingdom Conformity Assessment
Indicates the maximum and minimum temperature
limits at which the item shall be stored, transported
or used.
Atmospheric pressure limitation to which the
medical device can be safely exposed (operating)
This side up
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