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

GB | INSTRUCTIONS FOR USE
miniNAV

MEDICAL DEVICES CONSULTANTS

In compliance with the European Directive
concerning medical devices (Directive 93/42/
EEC), Christoph Miethke GmbH & Co. KG
has nominated 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
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/en/products/downloads/).

DIMENSIONS

Fig. 7: Schematic representation of the miniNAV with
its external dimensions
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