Data / Medical devices / Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass / France
FDA-registered makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass in France: 5 establishments
5 establishments in France are registered with the FDA to make Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass (product code DTL). 4 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
- Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- Product code
- DTL
- Country
- France
Makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Perouse Medical | FRANCE Oise, France | Manufacturer | 1 | April 23, 2008 | 0 | 0 | 0 | api.fda.gov |
| Sipa | Avesnes Sur Helpe Hauts-de-France, France | Manufacturer | 1 | November 27, 1981 | 0 | 0 | 0 | api.fda.gov |
| Sipv | Ecouen Ile-de-France, France | Manufacturer | 1 | November 27, 1981 | 0 | 0 | 0 | api.fda.gov |
| Vygon S A | ECOUEN 95440 Val-d'Oise, France | Manufacturer | 1 | November 27, 1981 | 0 | 0 | 0 | api.fda.gov |
| Arthesys | SACLAY Ile-de-France, France | Manufacturer | 0 | 0 | 0 | 0 | api.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.