Statistique de Rollerwerk Medical Engineering & Consulting

0Dispositifs total

0UDI-DI de base

0Non destinés au marché UE

0Certificats

0Valides

0Expirant < 6 mois

0Pays

Santé des certificats de Rollerwerk Medical Engineering & Consulting

Aucun certificat enregistré pour ce fabricant.

Aucun dispositif enregistré pour ce fabricant.

Mise à jour MD Atlas : le 27 mai 2026

DE-AR-000015883

Actif

Nom: DE/CA40 - Regierungspräsidium Tübingen Referat 25 - Sachgebiet Medizinprodukte
SRN: DE-CA-064
Téléphone: +49 7071 757 0
Email: Medizinprodukte@rpt.bwl.de

GERLACH Bettina
The conformity of the devices is checked in accordance with the QMS under which the devices are manufactured before a device is released. Fullfillment of reporting obligations acc. Articles 87 to 91 MDR In the case of investigational device, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued. The technical file and the EU declaration of conformity are drawn up and kept up to date (MDR §10(4) and 10 (6)). The PMS obligations are complied withaccording MDR §10 (10)
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