Vitame Ltd
GB-MF-000015647 · United Kingdom · Dartford
Vitame Ltd is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Among these devices, 8 are declared active.
Authorised representative in the Union: Elara Pharmaservices Europe Ltd.
Devices declared under this manufacturer
- ChloraEthyl Direkter Sprühstrahl
- Cryogesic Direct Stream
- Cryogesic Fine Spray
- Cyrogesic Fine Spray
- Dermogesic Non-Flammable Cold Spray (Fine Spray)
- Dermogesic Non-flammable Cold Spray (Direct Stream)
- Dermogesic non-flammable Cold Spray
Catalogue references include CHLORADIR100MLDE, CRYOGESICDIR100ML, CRYOGESICFIN100ML, DERMOGESIC100M, DERMOGESIC100ML, DERMOGESIFIN100ML.
European nomenclature codes declared: M9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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. Vitame Ltd was not found in either the U.S. or the Canadian register.