WAM
FR-MF-000007786 · France · Aix en Provence
WAM is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 26 |
|---|
Devices declared under this manufacturer
- Classic Tweezers
- Endo Tweezers
- Geko Tips
- Geko Tweezers
- Omnis
- Pâte Geko
- WAMAno
- WAMkey ® 1
- WAMkey ® 2
- WAMkey ® 3
- WAMkey ® intro Pack
- WAM’X Etriers
Showing 12 of 26 declared devices.
Catalogue references include CT, ET, OM1, OM2, WXE2, WXESQ2.
European nomenclature codes declared: Q010280.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. WAM was not found in either the U.S. or the Canadian register.