PELLET ASC
FR-MF-000041099 · France · Chaponnay
PELLET ASC is registered in the European database on medical devices as a manufacturer, with 198 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 198 |
|---|
Devices declared under this manufacturer
- ARSIS
- BARRE DROITE 50 CM, INOX BROSSÉ
- BARRE MANA
- Barre ARSIS d'appui 135°, 3PF, 400 x 400 mm, tube alu. anodisé Ø 38 x
- Barre ARSIS droite 400 mm, tube aluminium Oxyde Ø38x25 mm, cache-fixa
- Barre Barre droite 30 cm, aluminium époxy blancdroite 30 cm
- Barre Design droite 60 cm aluminium anodisé brillant, caches résine ch
- Barre Mana
- Barre d'appui verticale multifonctions H1050 mm, avec 3 accessoires, a
- Barre inox brossé
- CLASSIC
- ERGOLIFE
Showing 12 of 198 declared devices.
Catalogue references include 045140, 047630, 049220, 049430, 049436, 049449.
European nomenclature codes declared: Y181806, Y091203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 198 |
| 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 | 198 |
|---|---|
| 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. PELLET ASC was not found in either the U.S. or the Canadian register.