Data / Medical devices / Medical Device Data System / Germany

FDA-registered makers of Medical Device Data System in Germany: 20 establishments

Name: FDA-registered makers of Medical Device Data System in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

20 establishments in Germany are registered with the FDA to make Medical Device Data System (product code OUG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device: Medical Device Data System
Product code: OUG
Country: Germany

Makers of Medical Device Data System in Germany

Maker	Location	Role	Source
Ackermann Instrumente GMBH	RIETHEIM, WEILHEIM Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Adlink Technology GMBH	Deggendorf Bavaria, Germany	Manufacturer	api.fda.gov
B. Braun Avitum AG	MELSUNGEN Hesse, Germany	Manufacturer	api.fda.gov
Brainlab Se	Munich Bavaria, Germany	Exporter to the US, Manufacturer	api.fda.gov
Carl Zeiss Vision GMBH	AALEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
DMG Digital Enterprises Se	Hamburg, Germany	Manufacturer	api.fda.gov
Draeger Interservices GmbH	Luebeck Schleswig-Holstein, Germany	Contract manufacturer	api.fda.gov
Exocad GMBH	Darmstadt Hesse, Germany	Manufacturer	api.fda.gov
IBA Dosimetry GmbH	SCHWARZENBRUCK Bavaria, Germany	Manufacturer	api.fda.gov
Jaeger Medical GmbH	HOECHBERG Bavaria, Germany	Complaint file establishment, Manufacturer	api.fda.gov
Metasystems GMBH	ALTLUSSHEIM Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
ONCARE GmbH	Munich Bavaria, Germany	Complaint file establishment, Manufacturer	api.fda.gov
Philips Medizin Systeme Boeblingen GmbH	BOEBLINGEN Baden-Wurttemberg, Germany	Complaint file establishment, Manufacturer, Specification developer	api.fda.gov
Rein Medical GMBH	Moenchengladbach North Rhine-Westphalia, Germany	Manufacturer	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Roche Diagnostics GMBH	MANNHEIM Baden-Wurttemberg, Germany	Manufacturer, Specification developer	api.fda.gov
Seca	Hamburg, Germany	Manufacturer	api.fda.gov
Stryker Leibinger GMBH & Co. KG	FREIBURG Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Siemens Healthineers AG	ERLANGEN Bavaria, Germany	Contract manufacturer	api.fda.gov
eResearchTechnology GmbH	Estenfeld Bavaria, Germany	Complaint file establishment, Manufacturer	api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.