Ekobiff Sp. z o.o.
PL-MF-000045475 · Poland · Kobylnica
Ekobiff Sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Devices declared under this manufacturer
- PODKŁAD MEDYCZNY
- PODKŁAD MEDYCZNY MED SIM STANDARD
- PODKŁAD MEDYCZNY MILO COMFORT
Catalogue references include 40 cm x 50 m, 50 cm x 50 m, 50 cm x 80 m, 50cm x 40m, MILO5050, MILO5080.
European nomenclature codes declared: T99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Ekobiff Sp. z o.o. was not found in either the U.S. or the Canadian register.