D.M.D.
FR-MF-000012221 · France · Lezennes
D.M.D. is registered in the European database on medical devices as a manufacturer, with 68 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 19 |
|---|---|
| Class IIa | 49 |
Devices declared under this manufacturer
- BANDELETTES DENTASEPT ULTRA
- DENTASEPT 3H RAPID
- DENTASEPT ASPIRATION AF+
- DENTASEPT SH PRO
- DENTASEPT SH PRO WIPES
- DENTASEPT SPECIAL ROTATIVE
- DENTASEPT TRI ENZYMATIC
- DISINFECTANT DETERGENT SPRAY
- Dentasept Spray 60 pro
- Disinfectant Detergent Aspiration
- IGOSAFE INSTRUMENTS
- NORMOBIOT TRI ENZIMÁTICO NF
Showing 12 of 68 declared devices.
Catalogue references include 2462042BT, 24755006D, 2475500BL, 2536137AJ, 2536137B6, 25800472J.
European nomenclature codes declared: D0901, D99, D0701, V80, D01010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 68 |
| 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 | 68 |
|---|---|
| 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. D.M.D. was not found in either the U.S. or the Canadian register.