Bowil Biotech sp. z o.o.
PL-MF-000010555 · Poland · Władysławowo
Bowil Biotech sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 23 |
|---|
Most frequent device types declared: CelMat_10x10_H (PL), CelMat_10x20 (EN), CelMat_10x20 (PL), CelMat_10x20_H (EN), CelMat_E (EN).
Among these devices, 23 are declared sterile.
Devices declared under this manufacturer
- CelMat
Showing 12 of 23 declared devices.
Catalogue references include CelMat, CelMat H.
European nomenclature codes declared: M040404.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 23 |
| 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 | 23 |
|---|---|
| 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. Bowil Biotech sp. z o.o. was not found in either the U.S. or the Canadian register.