Mobilex A/S
DK-MF-000021885 · Denmark · Skanderborg
Mobilex A/S is registered in the European database on medical devices as a manufacturer, with 312 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 312 |
|---|
Most frequent device types declared: Dolphin aluminium wheelchair, Grab bar, Jaguar indoor rollator, Leopard rollator, Panda Royal rollator.
Among these devices, 5 are declared active.
Devices declared under this manufacturer
- Back for shower stool
- Dolphin wheelchair
- Grab bar, white, 50 cm
- Jaguar SUPREME rollator
- Leopard rollator (DK)
- Marlin wheelchair
- Marlin wheelchair with PU tires
- Pedal trainer With LCD Display
- Rubberramp, grey, with glue, 56 x 300 x 900 mm
- Rubberramp, grey, without glue, 56 x 300 x 1000 mm
- Singlefolded ramp, 77 x 120 cm
- Support rail 60 cm, black powder coated
Showing 12 of 312 declared devices.
Catalogue references include 271248, 271344, 302069, 302075, 306560, 306562.
European nomenclature codes declared: Y183015, Y120612, Y091203, Y122103,Y122106, Y181806, V080399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 312 |
| 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 | 312 |
|---|---|
| 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. Mobilex A/S was not found in either the U.S. or the Canadian register.