MG MICALLEF
FR-MF-000052601 · France · bordeaux
MG MICALLEF is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Devices declared under this manufacturer
- Bouillotte Sèche Calin
- Bouillotte Sèche Cervicale
- Bouillotte Sèche Dorsale
- Bouillotte Sèche Dualtherm
- Bouillotte Sèche Mini
Catalogue references include Bouillotte Sèche Calin, Bouillotte Sèche Cervicale, Bouillotte Sèche Dorsale, Bouillotte Sèche Dualtherm, Bouillotte Sèche Mini.
European nomenclature codes declared: M9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. MG MICALLEF was not found in either the U.S. or the Canadian register.