User Controls & System Status Indicators - CAIRE Companion 5 Manuel D'utilisation

Masquer les pouces Voir aussi pour Companion 5:
Table des Matières

Publicité

Les langues disponibles
  • FR

Les langues disponibles

  • FRANÇAIS, page 24
Companion 5
User Controls & System Status Indicators
Internal Symbols
0
Oxygen Output
2
I/O
On/Off Switch
No serviceable parts inside. Do not
open cover.
Keep away from flammable materials,
oil and grease.
ISO 7000; Graphical symbols for use on
equipment—Index and synopsis
Storage or operating temperature
range. Reg. # 0632
Storage humidity range. Reg. # 2620
Name and address of manufacturer.
Reg. # 3082
Date of manufacture. Reg. # 2497
Catalog Number. Reg. # 2493
Serial Number. Reg. # 2498
This way up. Reg. # 0623
Fragile, handle with care. Reg. #
0621
Keep away from rain, keep dry. Reg.
# 0626
Read user's manual before operation.
Reg. # 1641
Caution, consult accompanying docu-
ments. Reg. # 0434A
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
Warning. Reg. # W001
2 - ENG PN 21420526-C4 B | User Manual
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
Type BF applied part (degree of
protection against electric shock).
Reg. # 5333
QPS
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.
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.
Council Directive 2012/19/EU: waste electrical and
electronic equipment (WEEE)
WEEE
IEC 60601-1: Medical electrical equipment Part 1
General requirements for basic safety and essen-
tial performance
Drip Proof Equipment-IP21: The
Companion 5 provides protection
IP21
against the harmful effects of the
ingress of liquids. (IP21, per IEC
60529)

Publicité

Table des Matières
loading

Table des Matières