CAIRE Eclipse 5 Manuel D'utilisation page 2

Eclipse 5
User Controls & System Status Indicators
Internal Symbols
External Power Indicator
Power Cartridge (battery) Status
Gauge
Power Cartridge Symbol
A
Amperes
0
Oxygen Output
2
Recycle Symbol
FAA Approved Symbol: The U.S.
Federal Aviation Administration
(FAA) has approved this device for
use on-board commercial aircraft.
Flow Setting Indicator
Pulse Mode Operation
Device operating normally; power
button
Increase Flow Setting
Decrease Flow Setting
ISO 7000; Graphical symbols for use on
equipment—Index and synopsis
Storage or operating temperature
range. Reg. # 0632
Storage humidity range. Reg. # 2620
Atmospheric pressure limitation. Reg.
# 2621
Operator's manual; operating instruc-
tions. Reg. # 1641
Name and address of manufacturer.
Reg. # 3082
Date of manufacturer. Reg. # 2497
Catalog Number. Reg. # 2493
Serial Number. Reg. # 2498
This way up. Reg. # 0623
2 - ENG PN 21182453-C4 F | User Manual
Fragile, handle with care. Reg. #
0621
Keep away from rain, keep dry. Reg.
# 0626
Stacking limit by number. Reg. # 2403
ISO 7010: Graphical symbols—Safety colors
and safety signs—Registered safety signs
The instruction manual must be read.
Reg. # M002
Keep away from open flame, fire,
sparks. Open ignition source and
smoking prohibited. Reg. # P003
Do not smoke near unit or while
operating unit. Reg. # P002
Council Directive 93/42/EEC; concerning
medical devices
Authorized representative in the
European Community
If the product unique device identifier
(UDI) label has the CE#### symbol
on it, the device complies with the
requirements of Directive 93/42/EEC
concerning medical devices. The
CE#### symbol indicates notified
body number.
IEC 60417
Class II Equipment, Double Insulat-
ed Reg. # 5172
Alternating Current Reg. # 5032
Direct Current Reg. # 5031
Type BF applied part (degree of
protection against electric shock).
Reg. # 5333
CSA Certification
Certified for both the U.S. and Cana-
dian markets, to the applicable U.S.
and Canadian standards.
FCC Notice
21 CFR 801.15: Code of Federal Regulations
Title 21
Federal law restricts this device to
sale by or on the order of a physician.