Statistique de Resorba Medical GmbH

1Dispositifs total

1UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

1Pays

Santé des certificats de Resorba Medical GmbH

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
DK1010	`DK1010`	`+E203DK1010`	1	Sur le marché

Dispositifs placés dans 1 pays

Mise à jour MD Atlas : le 27 mai 2026

DE-MF-000009480

Actif

TOPPING Helen
- The post market surveillance obligations are compiled with in accordance with Article 10(10); - The reporting obligations referred to in Articles 87 to 91 are fulfilled; in the case of investigational devices, the statement referred to in section 4.1 of Chapter II of Annex XV is issued; - The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date.
Masqué
REYNOLDS Lynaye
Ensuring the conformity of devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released.
Masqué
WERSCHKY Anja
Ensuring the conformity of devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released.
Masqué