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Data / Medical devices / Catheter, Continuous Flush / Ireland

FDA-registered makers of Catheter, Continuous Flush in Ireland: 5 establishments

5 establishments in Ireland are registered with the FDA to make Catheter, Continuous Flush (product code KRA). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Catheter, Continuous Flush
Product code
KRA
Country
Ireland

Makers of Catheter, Continuous Flush in Ireland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boston Scientific LimitedCORK Munster, IrelandManufacturer6May 15, 2026010api.fda.gov
Boston Scientific LimitedGALWAY Galway(County), IrelandManufacturer5May 15, 2026000api.fda.gov
Stryker NeurovascularCork Munster, IrelandManufacturer1August 3, 2000000api.fda.gov
Merit Medical Ireland, LtdGalway Galway(County), IrelandManufacturer0000api.fda.gov
Vetex Medical LimitedBallinasloe Galway(County), IrelandSpecification developer0000api.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.