Hilding Anders Polska Sp. z o.o.
PL-MF-000032133 · Poland · Murowana Goślina
Hilding Anders Polska 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 IIa | 23 |
|---|
Most frequent device types declared: Materac medyczny, RUMBA VELUR 80x200.
Devices declared under this manufacturer
- FANDANGO MEDI-COVER 80x200
- MAKARENA ELIPS 160x200
- MAKARENA MERCED 160x200
- MAKARENA MERCED 80x200
- PASODOBLE TENCEL 80x200
- PASODOBLE VELVET 160x200
- PASODOBLE VELVET 80x200
- RUMBA ELIPS 160x200
- RUMBA VELUR
- RUMBA VELUR 80x200 N
- SALSA TENCEL 160x200
- SALSA VELVET 160x200
Showing 12 of 23 declared devices.
Catalogue references include G0B2A1C016, G0B2A1D016, G0B2A2D016, G0B2B1C008, G0B2C2C008, G0B2C2C016.
European nomenclature codes declared: V9099.
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. Hilding Anders Polska Sp. z o.o. was not found in either the U.S. or the Canadian register.