Breckle Matratzenwerk Weida
DE-MF-000010222 · Germany · Weida OT Hohenölsen
Breckle Matratzenwerk Weida is registered in the European database on medical devices as a manufacturer, with 355 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 355 |
|---|
Devices declared under this manufacturer
- Aqua12 302
- Aqua14 304
- BR-MNS 1004
- Bettverl.18 302
- Bretex Med12 LLQ 302
- Medi Kombi12 304
- Medi Kombi16 302
- Poly Med12 302 Bock
- Poly Med16 302
- Poly Standard12 310
- ViscoMatt Komfort14 302
- comfort-care I 12 304/310 H2
Showing 12 of 355 declared devices.
Catalogue references include Aqua12 302 087/208, Aqua14 304 087/200, BR-MNS 1004, Bettverl.18 302 020/100, Medi Kombi12 304 086/200, Medi Kombi16 302 100/200.
European nomenclature codes declared: V080702, T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 355 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 355 |
|---|---|
| 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. Breckle Matratzenwerk Weida was not found in either the U.S. or the Canadian register.