DELTEX
FR-MF-000002872 · France · PARIS
DELTEX is registered in the European database on medical devices as a manufacturer, with 373 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 373 |
|---|
Among these devices, 3 are declared sterile, 373 implantable, 1 with a measuring function.
Devices declared under this manufacturer
- DELTEX
Showing 12 of 373 declared devices.
Catalogue references include 2801608, 4930003, 5020026, 6120006, 6120611, 6120804.
European nomenclature codes declared: P0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 373 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 373 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. DELTEX was not found in either the U.S. or the Canadian register.