Cobi Rehab A/S
DK-MF-000001370 · Denmark · Karlslunde
Cobi Rehab A/S is registered in the European database on medical devices as a manufacturer, with 207 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 207 |
|---|
Most frequent device types declared: 0115-055-000, 0130-071-000, 0142-061-000, 0150-061-000, 0200-000-000.
Devices declared under this manufacturer
- Bariatric Wheelchair Viscocomfort Cushion 61cm
- Bariatric Wheelchair Viscocomfort Cushion 71cm
- Cobi Basic Viscoelastisk Skum 200x90x14
- Cobi Cruise 65
- Cobi U–cushion
- Cobi hygiejnepuder
- Cobi universal pude N
- Collar float, XS
- Crutch with anatomical grip left
- Dental underbenspude/voksen
- Float Stabilizer, S
- Modul C Sædepude, str. S
Showing 12 of 207 declared devices.
Catalogue references include 0233-061-050, 0233-071-050, 0316-4131-000, 0400-034-000, 0400-072-000, 3002-9017-000.
European nomenclature codes declared: V080302, V080702, Y122103, Y122127, Y091203, V080399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 207 |
| 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 | 207 |
|---|---|
| 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. Cobi Rehab A/S was not found in either the U.S. or the Canadian register.