Statistique de INNOTERE

1Dispositifs total

1UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

1Pays

Santé des certificats de INNOTERE

Aucun certificat enregistré pour ce fabricant.

Affichage de 1–1 sur 1 dispositifs.

Dénomination commerciale	Numéro de référence/catalogue	Code d'UDI-DI	Quantité	Statut
111VX2, 211IP1, 211IP2, 231IP1, 311IP1, 311IP2	`111VX2, 211IP1, 211IP2, 231IP1, 311IP1, 311IP2`	`++EINNPCT3`	1	Sur le marché

Dispositifs placés dans 1 pays

Mise à jour EUDAMED : le 23 févr. 2026

DE-MF-000006515

Actif

HEINEMANN Dr. Sascha
- Confirmation of conformity and release of the products (placing on the market). - Ensure that post-market surveillance obligations are fulfilled including reporting obligations - MDR Articles 87-91. - Ensuring that the technical documentation (TDs) and the EU declarations of conformity are properly prepared and that they are properly updated/amended as necessary (MDR Art. 15 Para. 3 No. b) - Approval of the manufacturing documentation for each custom-made product
Masqué
TAUCHERT Rica
- Verify the conformity of the products (articles, intermediate and final products) in an appropriate manner according to the company's own QMS, prior to release. - Collecting and evaluating reports of risks - Reporting and analysis of serious incidents and safety corrective actions and trends in the field (Articles 87, 88 and 89) - custom-made product: the appropriate documentation is available, the declaration is prepared in accordance with Annex XIII MDR
Masqué