Dirigeants et représentants réglementaires de AF Pharma Service Europe SL
DUGUINE Maria
Ensuring that:
The conformity of medical devices is checked in accordance with the QM system (before delivery) (Article 10(9)).
The technical documentation is kept up to date (Article 10(4) and (6)).
Market surveillance is performed in compliance with the EU regulations (Article 10(10)).
The reporting obligations according to the EU regulations are met (Article 10(13)).
For “investigational devices”, the statement according to Annex XV, Chapter 2 is issued.
Masqué
Catalogue des dispositifs de AF Pharma Service Europe SL
Aucun dispositif enregistré pour ce fabricant.
Santé des certificats de AF Pharma Service Europe SL