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Data / Medical devices / Bottle, Collection, Vacuum / Germany

FDA-registered makers of Bottle, Collection, Vacuum in Germany: 7 establishments

7 establishments in Germany are registered with the FDA to make Bottle, Collection, Vacuum (product code KDQ). 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
Bottle, Collection, Vacuum
Product code
KDQ
Country
Germany

Makers of Bottle, Collection, Vacuum in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
B. Braun Melsungen AGMELSUNGEN Hesse, GermanyContract sterilizer, Exporter to the US, Specification developer0000api.fda.gov
Draeger Interservices GmbHLuebeck Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Draegerwerk AG & Co. KGaALUEBECK Schleswig-Holstein, GermanySpecification developer0000api.fda.gov
GPE MedTech Systeme GmbHDassow Mecklenburg-Western Pomerania, GermanyContract manufacturer0000api.fda.gov
Medi-Globe GMBHAchenmuhle, Germany Bavaria, GermanyManufacturer0000api.fda.gov
Rommelag CDMO GmbHSulzbach-Laufen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
pfm medical mepro gmbhNonnweiler-Otzenhausen Saarland, GermanyComplaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer0000api.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.