This document is composed of one unique form with 6 sections.

We ask that you carefully review each of these sections to ensure that you have completed the element(s) applicable to your company's transition plan




1 General information

Applicable to everyone

2 Existing certification

Applicable to everyone

3. Class 1 Reusable Surgical Instrument(s)

Only applicable to manufacturers who intend to put on the market after May 26, 2020 at least one Class 1 Reusable surgical instrument subject to an initial certification under the (EU) 2017/745 implying the intervention of a Notified Body

4. MDD Class I being up-classified under the MDR

Only applicable to manufacturers who have Class I medical device(s) under Directive 93/42/EEC subject to an initial certification under the EU MDR 2017/745 because of the upgrade of its classification

5. Transitional Modalities

Applicable to everyone

6. Transitional Timeline to MDR

Applicable to everyone



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