Freudenberg Medical InHealth Technologies Blom-Singer Instrucciones De Uso página 93

STANDARD
SYMBOL
EN ISO 15223-
1:2016
93/42/EEC
EU 2017/745
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
EN ISO 15223-
1:2016
SYMBOLS GLOSSARY (USA only)
SYMBOL TITLE
No. & REF No.
Manufacturer;
5.1.1
CE Marking;
93/42/EEC
Annex XII,
EU 2017/745
Annex V
Authorized
representative
in the European
Community;
5.1.2
Catalogue
number; 5.1.6
Batch code;
5.1.5
Use-by date;
5.1.4
Date of
manufacture;
5.1.3
Caution; 5.4.4
Do not use
if package is
damaged; 5.2.8
Consult
instructions for
use; 5.4.3
Non-sterile;
5.2.7
Blom‑Singer Laryngectomy Tubes Instructions for Use
®
MEANING OF SYMBOL
Indicates the medical device manufacturer, as
defined in EU Directives or Regulations
CE marking of conformity
Indicates the authorized representative in the
European Community
Indicates the manufacturer's catalogue
number so that the medical device can be
identified
Indicates the manufacturer's batch code so
that the batch or lot can be identified
Indicates the date after which the medical
device is not to be used
Indicates the date when the medical device
was manufactured
Indicates the need for the user to consult the
instructions for use for important cautionary
information such as warnings and precautions
that cannot, for a variety of reasons, be
presented on the medical device itself
Indicates a medical device that should not
be used if the package has been damaged
or opened
Indicates the need for the user to consult the
instructions for use
Indicates a medical device that has not been
subjected to a sterilization process
37889-01B I 93