Endo Endoengineering Srl
Registration Of Medical Devices To The Ministry Of Health
The DM 21 December 2009 establishes the obligation to register in the medical devices database uses new methods. Registration is mandatory for all manufacturers and other entities responsible for placing devices on the Italian market for Class I, IIa, IIb and III, kits and assemblies and active implantable devices.
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Endo Engineering has the expertise required to stand by at all stages of registration and provides support in the following activities:
- registration of the manufacturer and the authorized representative;
- GMDN classification and identification of CND of your product;
- document review;
- handle all the paperwork.