You are on page 1of 1

MDR Conformity Assessment Procedure CLASS I

Annex I General Safety and Performance Requirements


Annex II Technical Documentation
Annex III Technical Documentation on Post Market Surveillance
Annex IV EU Declaration of Conformity
Annex VI UDI – Unique Device Identification
Annex VIII Classification Rules

MEDCERT Form Nr. 520102EN / Rev. 1 / 2017.11.07

You might also like