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Symbol
(ISO 15223-1, 5.1.1)
Authorized Representative in
the European Community (ISO
Date of manufacture
(ISO 15223-1, 5.1.3)
(ISO 15223-1, 5.1.4)
(ISO 15223-1, 5.1.5)
(ISO 15223-1, 5.1.6)
Sterilized using ethylene oxide
(ISO 15223-1, 5.2.3)
Do not use if package is
(ISO 15223-1, 5.2.8)
Keep away from sunlight
(ISO 15223-1, 5.3.2)
(ISO 15223-1, 5.4.2)
Consult instructions for use
(ISO 15223-1, 5.4.3)
Contains or presence of
natural rubber latex
(ISO 15223-1, 5.4.5)
Not made with natural rubber
(ISO 15223-1, 5.4.5 and
European Conformity
(EU MDR 2017/745, Article
(MedTech Europe Guidance:
Use of Symbols to Indicate
Compliance with the MDR)
Title of Symbol
Manufacturer
15223-1, 5.1.2)
Use-by date
Batch code
Catalog number
damaged
Do not reuse
latex
Annex B)
20)
Medical Device
Quantity
(IEC 60878, 2794)
Disposable Endocavity Needle Guide
Description of Symbol
Indicates the medical device manufacturer.
Indicates the Authorized Representative in the European
Indicates the date when the medical device was manufactured.
Indicates the date after which the medical device is not to be used.
Indicates the manufacturer's batch code so that the batch or lot
Indicates the manufacturer's catalogue number so that the
medical device can be identified.
Indicates a medical device that has been sterilized using ethylene
Indicates a medical device that should not be used if the package
has been damaged or opened.
Indicates a medical device that needs protection from light
Indicates a medical device that is intended for one use, or for use
on a single patient during a single procedure.
Indicates the need for the user to consult the instructions for use.
Indicates the presence of natural rubber or dry natural rubber
latex as a material in the construction within the medical device or
the packaging of a medical device.
Indicates that natural rubber latex was not used in the
manufacturing of the product, its container, or its packaging.
Indicates manufacturer declaration that the product complies with
the essential requirements of the relevant European health, safety
and environment protection legislation.
Indicates the product is a medical device.
To indicate the number of pieces in the package.
4
Community.
can be identified.
oxide.
sources.
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