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Data / Medical devices / Catheter, Irrigation / Germany

FDA-registered makers of Catheter, Irrigation in Germany: 9 establishments

9 establishments in Germany are registered with the FDA to make Catheter, Irrigation (product code GBX). 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
Catheter, Irrigation
Product code
GBX
Country
Germany

Makers of Catheter, Irrigation in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aesculap AGTUTTLINGEN, DONAU Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Asanus Medizintechnik GMBHNEUHAUSEN OBECK Baden-Wurttemberg, GermanyManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Assamed GMBHBEXBACH Saarland, GermanyManufacturer0000api.fda.gov
Fresenius Kabi Deutschland GMBHBAD HERSFELD Hesse, GermanySpecification developer0000api.fda.gov
Medicon, E.G.TUTTLINGEN Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Pemax Kunststoff GMBHStuttgart Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
RoweMed AG - Medical 4 LifeParchim Mecklenburg-Western Pomerania, GermanyContract manufacturer0000api.fda.gov
Sanner GMBHBensheim Hesse, GermanyContract manufacturer0000api.fda.gov
Teufel & Gerlach GmbHTuttlingen Baden-Wurttemberg, 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.