Sterilization | Packaging; Medical Devices Consultants; Requirements Of The Mdd (Directive 93/42/Eec) - MIETHKE Ventricular Catheter Mode D'emploi

GB | INSTRUCTIONS FOR USE

STERILIZATION | PACKAGING

All products are carefully and thoroughly
steam sterilized. Owing to the fact that the
product is packaged in two layers of sterile
packaging, five years of sterility are guaran-
teed. The expiration date for each item is indi-
cated on the package. If the packaging is
damaged in any way, the product should not
be used under any circumstances.
The functional safety and reliability of resteril-
ized products cannot be guaranteed.

MEDICAL DEVICES CONSULTANTS

In compliance with
on medical devices (directive 93/42/EEC),
Christoph Miethke GmbH & Co. KG has nom-
inated medical products consultants as con-
tacts for all product-related questions.
You can reach
consultants at:
Phone +49 331 62083-0
info@miethke.com
8
European directive
our medical devices
Ventricular Catheter / Peritoneal Catheter
REQUIREMENTS OF THE MDD
(DIRECTIVE 93/42/EEC)
The Medical Device Directive requires com-
prehensive documentation of the where-
abouts of medical devices used in humans,
especially for implants. The individual iden-
tification number of the implanted valve
should therefore be recorded in the patient's
medical records and patient passport to
ensure complete traceability. Translations
of these instructions for use into addi-
tional languages can be found on our
website (https://www.miethke.com/en/prod-
ucts/downloads).