Civco OMNITRAX Bedienungsanleitung Seite 3

omniTRAX™ Active Patient Tracker
Symbol Title of Symbol
(ISO 15223-1, 5.1.1)
Authorized Representative in the
European Community (ISO
15223-1, 5.1.2)
Date of manufacture
(ISO 15223-1, 5.1.3)
(ISO 15223-1, 5.1.4)
(ISO 15223-1, 5.1.5)
Catalog number
(ISO 15223-1, 5.1.6)
Do not use if package is
(ISO 15223-1, 5.2.8)
Keep away from sunlight
(ISO 15223-1, 5.3.2)
Single patient multiple use
(ISO 7000, 3706)
Consult instructions for use
(ISO 15223-1, 5.4.3)
Not made with natural rubber
(ISO 15223-1, 5.4.5 and Annex
European Conformity
(EU MDR 2017/745, Article 20)
(MedTech Europe Guidance:
Use of Symbols to Indicate
Compliance with the MDR)
(IEC 60878, 2794)
Manufacturer
Use-by date
Batch code
damaged
latex
B)
Medical Device
Quantity
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 can
Indicates the manufacturer's catalogue number so that the medical
device can be identified.
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 sources.
Indicates the medical device may be used multiple times (multiple
procedures) on a single patient.
Indicates the need for the user to consult the instructions for use.
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.
1
Community.
be identified.
English