Data / Medical devices / France / Euro Diffusion Medicale
Euro Diffusion Medicale: FDA-registered device maker in Domont Ile-de-France, France, 1 510(k) clearance
Euro Diffusion Medicale is registered with the FDA (registration 3013181568) in Domont Ile-de-France, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 27, 2011. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013181568
- Address
- 1 Rue des Boisseliers, Domont Ile-de-France, France, 95330
- Owner or operator
- Euro Diffusion Medicale (10081182)
- Roles
- Exporter to the US
- First device listed
- March 23, 2021
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 27, 2011 | K101952 | KONIX ULTRASOUND GEL | ITX | Substantially Equivalent | Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa | accessdata.fda.gov |
Compare with other makers
Updated May 27, 2011. 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.