FDA applicant

Merck Millipore, Ltd.

Carrigtwohill, IE2 decisions2014–20150 recalls

FDA records 2 decisions for Merck Millipore, Ltd. (Carrigtwohill, IE) from 2014 to 2015: 2 510(k) clearances. Most are in product codes FPB (Filter, Infusion Line) and BSN (Filter, Conduction, Anesthetic). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Merck Millipore, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2014high 1 (2014) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Merck Millipore, Ltd. by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Merck”

FDA records each applicant name separately; these may or may not be the same firm.

Merck, Sharp & Dohme 4 Merck Biomaterial GmbH 1

Merck Millipore, Ltd.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Merck”