EUROTEKNIKA
FR-MF-000004032 · France · Sallanches
EUROTEKNIKA is registered in the European database on medical devices as a manufacturer, with 420 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 420 |
|---|
Most frequent device types declared: BL, CGC TG, S, TL.
Among these devices, 37 are declared sterile, 191 reusable.
Catalogue references include CCK_QH15.150, CEP_18.205, CMK_TR38, CMP_CG_35A.WP, ETK_UN.SBPO, IE_U.A1.
European nomenclature codes declared: Q010399, Q0199, Q010207, Q010280, P01020101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | EUROTEKNIKA (FR) · FDA 3007521935 |
| Devices in EUDAMED | 420 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 420 |
|---|---|
| Found in the U.S. device database | 17 |
| Share | 4.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | EUROTEKNIKA |
North American profile: Both markets. EUROTEKNIKA is registered in both the United States and Canada.