Statistique de Baxter Medical Systems GmbH + Co. KG

379Dispositifs total

31UDI-DI de base

0Non destinés au marché UE

1Certificats

1Valides

0Expirant < 6 mois

1Pays

Santé des certificats de Baxter Medical Systems GmbH + Co. KG

Aucun dispositif enregistré pour ce fabricant.

Dispositifs placés dans 1 pays

Mise à jour EUDAMED : le 20 avr. 2026

DE-MF-000005071

Actif

Nom: DE/CA90 - Thüringer Landesamt für Verbraucherschutz Dezernat 21 Technischer Verbraucherschutz, Marktüberwachung
SRN: DE-CA-059
Téléphone: +49-361 57-3815000
Email: poststelle@tlv.thueringen.de

DÄHNERT Marco
Ensuring conformity of the device is appropriately checked in accordance with the Quality Management System (QMS) before the device is released. Ensuring Post-Market Surveillance (PMS) obligations are met (ref. Article 10 (10) of MDR). Ensuring reporting obligations relating to vigilance are met (ref. Article 87 to 91 of MDR).
Masqué
SCHELL Bernd
Ensuring technical documentation and EU Declaration of Conformity (DoC) are drawn up and kept up to date. Ensuring that the Declaration for investigational device(s) used in clinical trials conforms to General Safety and Performance Requirements (GSPR) apart from aspects covered by the clinical investigation and every precaution has been taken to protect the health and safety of the subject (ref. Annex XV Chapter II Section 4.1 of MDR).
Masqué