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Standard
Symbol
Reference
ISO 7000
Symbol 1135
combined with a
battery chemistry
symbol to differentiate
battery type
21 CFR Part
Rx Only
801.109(b)(1)
ISO 15223-1
Symbol 5.4.5
LATEX
(Reference Annex
B for the general
prohibition symbol)
2012/19/EU
ISO 15223-1
Symbol 5.1.1
ISO 15223-1
Symbol 5.1.2
ISO 15223-1
Symbol 5.1.3
ISO 15223-1
Symbol 5.1.6
ISO 15223-1
Symbol 5.1.7
ISO 15223-1
Symbol 5.4.3
Annex A #A.15
ISO 15223-1
Symbol 5.4.4
IEC 60601-1
Table D.1 #10
ISO 60601-1
Table D.2 #2
ISO 15223-1
Symbol 5.2.8
ISO 15223-1
Symbol 5.3.7
ISO 15223-1
Symbol 5.3.8
ISO 15223-1
Symbol 5.3.9
Swiss Medical
Device Ordinance
CH
REP
(MedDO)
UKCA Medical
Device Regulation
(SI 2022 No 618,
as amended)
(UK MDR 2002)
Standard Title
Lithium-ion Recycling Symbol
Labeling-Prescription devices
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Waste Electrical and Electronic Equipment
(WEEE)
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical electrical equipment — Part 1:
General requirements for basic safety and
essential performance.
Medical electrical equipment — Part 1:
General requirements for basic safety and
Essential performance.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Medical devices — Symbols to be used
with medical device labels, labelling and
information to be supplied.
Swiss Medical Device (MedDO).
UKCA Medical Device Regulation.
Symbol Title
Recycling identification
Indicates the battery composition for
mark
recycling purposes.
Prescription only
Indicates the product is authorized for
sale by or on the order of a licensed
healthcare practitioner.
Not made with Natural
Indicates a medical device that is not
Rubber Latex
made with natural rubber latex.
Disposal at end
Indicates that electrical and electronic
of operating life
equipment waste should not be
instructions
discarded together with unseparated
waste but must be collected separately.
Manufacturer
Indicates the medical device
manufacturer.
Authorized
Indicates the Authorized representative
representative in the
in the European Community.
European Community
Date of manufacture
Indicates the date when the medical
device was manufactured.
Catalogue number
Indicates the manufacturer's catalogue
number so that the medical device can
be identified.
Serial number
Indicates the manufacturer's serial
number so that a specific medical
device can be identified.
Consult instructions for
Indicates an instruction to consult an
use
electronic instructions for use (eIFU).
Caution: Read
Indicates the need for the user to
all warnings and
consult the instructions for use for
precautions in
important cautionary information such
instructions for use
as warnings and precautions that
cannot, for a variety of reasons, be
presented on the medical device itself.
General warning sign
Indicates a hazard of potential personal
injury to patient or operator.
Do not use if package
Indicates a medical device that should
is damaged
not be used if the package has been
damaged or opened.
Temperature limit
Indicates the (storage) temperature
limits to which the medical device can
be safely exposed.
Humidity limitation
Indicates the range of (storage)
humidity to which the medical device
can be safely exposed.
Atmospheric pressure
Indicates the acceptable upper and
limitation
lower limits of atmospheric pressure for
transport and storage.
Indicates the Authorized
Indicates the Authorized Representative
Representative in
in Switzerland.
Switzerland
UKCA Mark
In compliance with the United Kingdom
technical conformity.
Explanation
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