Ferita Tytus Biegański
PL-MF-000027275 · Poland · Mokronos Dolny
Ferita Tytus Biegański is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 54 |
|---|
Devices declared under this manufacturer
- CODOPRIM
- CODOTEX
- DOZ MED CODONET
- HELTISO Codocare
- VELOTEX
Showing 12 of 54 declared devices.
Catalogue references include CODOPRIM elastyczna siatka opatrunkowa 4/TX-SO-0401 (1m), CODOTEX 14/TX-SO-1401 (1m), CODOTEX 3/TX-SO-0301(1m), Opaska elastyczna 4m x 15cm / TX-OT-0415, Opaska elastyczna 5m x 15cm / TX-OT-0515, VELOTEX 1/TX-SO-0110 (10m).
European nomenclature codes declared: M030499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 54 |
|---|---|
| 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. Ferita Tytus Biegański was not found in either the U.S. or the Canadian register.