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Data / Medical devices / Filter, Bacterial, Breathing-Circuit / Germany

FDA-registered makers of Filter, Bacterial, Breathing-Circuit in Germany: 6 establishments

6 establishments in Germany are registered with the FDA to make Filter, Bacterial, Breathing-Circuit (product code CAH). 2 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
Filter, Bacterial, Breathing-Circuit
Product code
CAH
Country
Germany

Makers of Filter, Bacterial, Breathing-Circuit in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Draegerwerk AG & Co. KGaALUEBECK Schleswig-Holstein, GermanyManufacturer, Specification developer2December 7, 2022000api.fda.gov
Jaeger Medical GmbHHOECHBERG Bavaria, GermanyComplaint file establishment, Manufacturer, Specification developer2October 17, 2011000api.fda.gov
Draeger Interservices GmbHLuebeck Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Ganshorn Medizin Electronic GMBHBad Neustadt Bavaria, GermanyManufacturer0000api.fda.gov
Riensch & Held GMBH & Co. KGHamburg, GermanyContract manufacturer0000api.fda.gov
Saint-Gobain Performance Plastics L+S GMBHNeuhaus am Rennweg Thuringia, GermanyContract 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.