FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Merck KGaALabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record. See the Merck KGaA group view.
As of Nov 15, 2026, FDA's public records list Merck Millipore Ltd. with 2 510(k) clearances and 1 device recall. The most recent is a device recall dated May 14, 2018: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 14, 2018 | Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concenClass II · In vitro diagnostic devices, used greater than 6 months after date of manufacture, may have increased concentration time | Device recalls |
| Aug 11, 2015 | Cathivex ¿GV filter unitsK143583 · FPB | 510(k) clearances |
| Mar 27, 2014 | VENTED MILLEX -GV, CATHIVEX -GVK133004 · BSN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
