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Les langues disponibles
SYMBOLS
The operator must read
this document (Instructions
for Use) before use.
Note: This symbol is blue
on the product label.
With respect to electric
shock, fire and mechanical
hazards only in
accordance with
CAN/CSA-C22.2 No.
60601-1 (2008) + (2014)
E348583
and ANSI/AAMI ES
CAN/CSA-C22.2
No 60601-1
60601-1 (2005) + AMD
(2008)+(2014)
and ANSI/AAMI
(2012)
ES 60601-1(2005)
+AMD(2012)
MEDICAL EQUIPMENT
Refer to this document
(Instructions for Use) for a
i
description of the product
classification (3rd Edition).
Refer to this document
(Instructions for Use) for a
description of the product
classification (2nd Edition).
CE marking indicating
conformity with European
Community harmonised
legislation
Figures indicate Notified
Body supervision.
Indicates the product is a
Medical Device according
to EU Medical Device
Regulation 2017/745
UK Symbol explanation
This section is only applicable to United Kingdom (UK) market when UK marking is applied to
the Arjo medical device labelling.
UK marking indicating conformity with UK Medical Devices Regulations
2002 (SI 2002 No 618, as amended).
Figures indicate UK Approved Body supervision.
UK Responsible Person & UK Importer:
Arjo (UK) Ltd, ArjoHuntleigh House, Houghton Regis. LU5 5XF
Is the appointed UK Responsible Person as defined in UK Medical Devices Regulations 2002
(SI 2002 No 618, as amended).
For Northern Ireland (NI) CE marking will still apply until further amendment to applicable
regulations.
Power
O (Off)
Disconnects from
the mains supply
Double Insulated
Serial Number
SN
Do not dispose of
in domestic refuse
Manufacturer:
This symbol is
accompanied by
the name and the
address of the
manufacturer.
Unique device
identifier
18
Power
I (On)
Connects to the
mains supply
Type BF
Model number
REF
Dangerous voltage
Date of Manufacture
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