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Los distintos grupos de trabajo finalizan diversas guías (se nos acumula la lectura):

MDCG 2021-13 rev.1 – «Questions and answers on obligations and related rules for the registration in EUDAMED of actors other than manufacturers, authorised representatives and importers subject to the obligations of Article 31 MDR and Article 28 IVDR» – July 2021 

MDCG 2021-14 – «Explanatory note on IVDR codes»  – July 2021

MDCG 2021-15  – «Application form to be submitted by a conformity assessment body when applying for designation as notified body under Regulation (EU) 2017/745 on medical   devices (MDR)» – July 2021

MDCG 2021-16  – «Application form to be submitted by a conformity assessment body when applying for designation as notified body under Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR)»  – July 2021

MDCG 2021-17 – «Applied for scope of designation and notification of a conformity assessment body – Regulation (EU) 2017/745 (MDR)» – July 2021

MDCG 2021-18 – «Applied for scope of designation and notification of a conformity assessment body – Regulation (EU) 2017/746 (IVDR)» – July 2021

MDCG 2021-19 – «Guidance note integration of the UDI within an organisation’s quality management system» – July 2021