PF mobility ApS
DK-MF-000018768 · Denmark · Vildbjerg
PF mobility ApS is registered in the European database on medical devices as a manufacturer, with 40 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 40 |
|---|
Among these devices, 32 are declared active.
Devices declared under this manufacturer
- Disco
- Disco Medi
- Disco Medi P20
- Disco P20
- Duo Reha
- Duo Reha P20
- Duo Reha P25
- Side by Side
- Side by Side P25
- Stabilo
- Stabilo P25
- Stabilo Small P20
Showing 12 of 40 declared devices.
Catalogue references include 5000230, 5000305, 5000306, 5000330, 5000390, 5000392.
European nomenclature codes declared: Y121806.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 40 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 40 |
|---|---|
| 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. PF mobility ApS was not found in either the U.S. or the Canadian register.