User Controls & System Status Indicators - CAIRE NewLife Series User Manual

NewLife Family
User Controls & System Status Indicators
ISO 7000; Graphical symbols for use on
equipment—Index and synopsis
Read user's manual before operation.
Reg. # 1641
Operating temperature limitation of
these units is 41°F to 104°F (5°C to
40°C). Storage temperature limitation
range is -13°F to +158°F (-25°C to
+70°C). Reg. # 0632
Humidity range is 10 to 95%. Reg.
# 2620
Atmospheric pressure limitation. Reg.
# 2621
Keep away from rain, keep dry. Reg.
# 0626
Name and address of manufacturer.
Reg. # 3082
Caution, consult accompanying docu-
ments. Reg. # 0434A
Catalog Number. Reg. # 2493
Serial Number. Reg. # 2498
This way up. Reg. # 0623
Fragile, handle with care. Reg. #
0621
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
Type BF applied part (degree of
protection against electric shock).
Reg. # 5333
Warning. Reg. # W001
Council Directive 93/42/EEC; concerning
medical devices
2 - ENG PN MN239 B | User Manual
Authorized representative in the
European Community
This device complies with the
requirements of Directive 93/42/EEC
concerning medical devices. It bears
the CE marking as shown.
Internal Symbols
Keep away from flammable materials,
oil and grease.
Safety agency for CAN/CSA
C22.2 No. 60601-1-14 for medical
electrical equipment. Certified for
both the U.S. and Canadian markets,
to the applicable U.S. and Canadian
standards.
Do not disassemble.
When present on the device alarm
panel indicates external power inter-
ruption has been detected.
When present on the device alarm
panel indicates low oxygen concen-
tration in device output.
ON (power switch on)
OFF (power switch off)
Date of Manufacture
Class II equipment
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.
IEC 60601-1: Medical electrical equipment Part
1 General requirements for basic safety and
essential performance
Drip Proof Equipment - IP21
Council Directive 2012/19/EU: waste electrical
and electronic equipment (WEEE)