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CAIRE VisionAire 5 - User Controls and System Status Indicators

CAIRE VisionAire 5
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2 - US PN MN238 E | User Manual
VisionAire 5
User Controls & System Status Indicators
ISO 7000
Read users manual before operation.
Reg. # 1641
Keep away from rain, keep dry. Reg.
# 0626
Stacking limit by number. Reg. # 2403
Name and address of manufacturer.
Reg. # 3082
The country and date of manufacture.
The “CC” identies the two letter
country code of the country of manu-
facture. The date of manufacture is in
YYYY-MM-DD format. Reg. # 6049
Caution, consult accompanying docu-
ments. Reg. # 0434A
Catalog Number. Reg. # 2493
Serial Number. Reg. # 2498
Storage or operating temperature
limitation range Reg. # 0632
Storage humidity range
Reg. # 2620
This way up. Reg. # 0623
Fragile, handle with care. Reg. #
0621
Contains hazardous substances. Reg.
# 3723
Importer. Reg. # 3725
ISO 7010
The instruction manual must be read.
Reg. # M002
Keep away from open ame, re,
sparks. Open ignition source and
smoking prohibited. Reg. # P003
Do not smoke near unit or while
operating unit. Reg. # P002
Type BF applied part (degree of
protection against electric shock).
Reg. # 5333
Warning. Reg. # W001
Council Directive 93/42/EEC
Authorized representative in the
European Community
If the product unique device identier
(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 notied
body number.
Additional Symbols
Keep away from ammable materials,
oil and grease.
Do not disassemble.
When present on the device alarm
panel indicates external power inter-
ruption has been detected.
2018 Labeling: When present on the
device alarm panel indicates low ox-
ygen concentration in device output.
ON (power switch on)
OFF (power switch off)
Authorized representative in
Switzerland.
If the device bears the UKCA mark
as shown with UKCA#### indicating
the notied body number, this device
complies with UKCA regulations.
IEC 60417
Class II equipment
21 CFR 801.15
Federal law restricts this device to
sale by or on the order of a physician.
IEC 60601-1
Drip Proof Equipment - IP21

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