3M 9681 Manual Del Usuario página 11

Symbol Glossary
Symbol Title
Manufacturer
Authorized Representative
in European Community
Date of Manufacture
Catalogue number
Temperature limit
Do not re‑use
Consult instructions for use
Caution
Medical Device
Importer
CE Mark
Use Indoors
Symbol
Indicates the medical device manufacturer
as defined in Medical Device Regulation (EU)
2017/745 formerly EU Directive 93/42/EEC.
Indicates the authorized representative in the
European Community. Source: ISO 15223, 5.1.2,
Indicates the date when the medical device was
manufactured. Source: ISO 15223, 5.1.3
Indicates the manufacturer's catalogue number so
that the medical device can be identified. Source :
Indicates the temperature limits to which the
medical device can be safely exposed. Source: ISO
Indicates a medical device that is intended for one
use or for use on a single patient during a single
Indicates the need for the user to consult the
instructions for use. Source: ISO 15223, 5.4.3
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. Source: ISO 15223, 5.4.4
Indicates the entity importing the medical device
Indicates conformity to all applicable European
Union Medical Device Regulations and Directives.
Indicates medical device be used indoors
10
Description and Reference
Source: ISO 15223, 5.1.1
2014/35/EU, and/or 2014/30/EU
ISO 15223, 5.1.6
15223, 5.3.7
procedure. Source: ISO 15223, 5.4.2
Indicates the item is a medical device.
into the EU.