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Data / Medical devices / Filter, Bacterial, Breathing-Circuit / United Kingdom

FDA-registered makers of Filter, Bacterial, Breathing-Circuit in the United Kingdom: 7 establishments

7 establishments in the United Kingdom are registered with the FDA to make Filter, Bacterial, Breathing-Circuit (product code CAH). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Filter, Bacterial, Breathing-Circuit
Product code
CAH
Country
United Kingdom

Makers of Filter, Bacterial, Breathing-Circuit in the United Kingdom

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Intersurgical Ltd.Wokingham, Berkshire, United KingdomManufacturer, Specification developer10June 15, 2023000api.fda.gov
Flexicare Medical Ltd.RHONDDA CYNON TAFF Wales, United KingdomSpecification developer6March 23, 2020000api.fda.gov
Pall NewquayNewquay Cornwall, United KingdomManufacturer3November 16, 2021000api.fda.gov
ConvaTec Limited, GDC BuildingDeeside Flintshire, United KingdomSpecification developer1November 30, 1994000api.fda.gov
GVS Filter Technology UK LtdLancaster Lancashire, United KingdomManufacturer, Specification developer1May 13, 2004000api.fda.gov
KoKo PFT LTD.Waltham Abbey Essex, United KingdomManufacturer1October 21, 1993000api.fda.gov
MD Diagnostics LtdChatham Kent, United KingdomManufacturer1September 25, 2019000api.fda.gov

Updated November 3, 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.