Sterilisation; Requirements Of The Medical Device Directive (Directive 93/42/Eec); Medical Devices Consultants; Dimensions - MIETHKE M.blue Mode D'emploi

INSTRUCTIONS FOR USE | EN
M.blue
®

STERILISATION

The products are sterilised with steam under
strictly controlled conditions. The expiry date
is printed on the wrapping of each individ-
ual product. If the packaging is damaged, the
product must not be used in any circum-
stances. No guarantee can be given for the
functional safety and reliability of resterilised
products.
REQUIREMENTS OF THE
MEDICAL DEVICE DIRECTIVE
(DIRECTIVE 93/42/EEC)
The Medical Device Directive requires com-
prehensive documentation of the fate of med-
ical devices used in humans, especially for
implants. The individual implant identification
number should therefore be recorded in the
patient's medical records and patient card to
ensure complete traceability. Translations of
these instructions for use into additional lan-
guages can be found on our website:
https://www.miethke.com/downloads/

MEDICAL DEVICES CONSULTANTS

In compliance with the European Directive con-
cerning medical devices (Directive 93/42/EEC),
Christoph Miethke GmbH & Co. KG has nomi-
nated medical devices consultants as contacts
for all product-related questions.
You can contact our medical devices consul-
tants via:
Tel. +49 331 62083-0
info@miethke.com

DIMENSIONS

29