Statistics for Baxter Medical Systems GmbH + Co. KG

379Total Devices

31Basic UDI-DIs

0Not destined for EU market

1Certificates

1Valid

0Expiring < 6 months

1Countries

Certificate health for Baxter Medical Systems GmbH + Co. KG

No devices registered for this manufacturer.

Devices placed in 1 country

EUDAMED update: Apr 20, 2026

DE-MF-000005071

Active

Name: DE/CA90 - Thüringer Landesamt für Verbraucherschutz Dezernat 21 Technischer Verbraucherschutz, Marktüberwachung
SRN: DE-CA-059
Phone: +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).
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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).
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