ML FUSION
FR-MF-000020822 · France · LA COUTURE
ML FUSION is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Most frequent device types declared: fauteuil, machine, table.
Devices declared under this manufacturer
- Fauteuil de rééducation du genou quadriergoforme Classique - dossier i
- Fauteuil de rééducation du genou quadriergoforme Classique - dossier r
- Poulie universelle 40 kg avec double système - solo
- Poulie universelle 50 kg - solo
- Poulie universelle 50 kg avec double système - solo
- Poulie universelle 60 kg - solo
- Presse horizontale à charge frontale dossier non réglable 100 kg
- Presse horizontale à charge frontale dossier réglable 100 kg
- Presse horizontale à charge latérale dossier réglable 100 kg avec cart
- Presse horizontale à charge latérale dossier réglable 120 kg avec cart
- Presse horizontale à charge latérale dossier réglable 80 kg avec carte
- Table d'examen 4 plans - dossier proclive - fessier large - 2 jambière
Showing 12 of 27 declared devices.
Catalogue references include DK50C, DK75A, KIN50, PRE752, PRE753, PRE754.
European nomenclature codes declared: Z120616.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. ML FUSION was not found in either the U.S. or the Canadian register.