Biomar Sp. z o.o.
PL-MF-000024783 · Poland · Pabianice
Biomar Sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 43 |
|---|
Most frequent device types declared: Opaski podtrzymujące dziane.
Devices declared under this manufacturer
- CEPHAMED Opaska dziana podtrzymująca
- Opaska dziana podtrzymująca APTEO
- Opaska dziana podtrzymująca BIOMAR
- Opaska dziana podtrzymująca OMET MEDICAL
- Opaska elastyczna uciskowa tkana z zapinką pakowana w kartonik
- Opaska elastyczna uciskowa tkana z zapinką pakowana w papier PE
- safeLINE BAND Opaska dziana podtrzymująca niejałowa
- safeLINE ELASTIC Opaska elastyczna uciskowa tkana z zapinka, niejałowa
- safeLINE ELASTIC Opaska elastyczna uciskowa tkana z zapinką, niejałowa
Showing 12 of 43 declared devices.
Catalogue references include B OEP 155, B OEP 104, BOD054, OB10111504_5387, OL10210804_5387, OL10211005_5387.
European nomenclature codes declared: M0303010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| 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 | 43 |
|---|---|
| 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. Biomar Sp. z o.o. was not found in either the U.S. or the Canadian register.