Motherhood Sp. z o.o.
PL-MF-000027049 · Poland · Warszawa
Motherhood Sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: FASOLKA PREMIUM, FASOLKA STANDARD, KOJEC MEDICAL, KOJEC STANDARD, Kojec Premium.
Devices declared under this manufacturer
- ALL-COTTON WATERPROOF PAD 120X65
- ALL-COTTON WATERPROOF PAD 195X160
- ALL-COTTON WATERPROOF PAD 195X90
- ALL-COTTON WATERPROOF PAD 90X65
- KOJEC PREMIUM
- KOJEC STANDARD
- MEDICAL SLEEPY-C
- NURSING SUPPORT PILLOW
- NURSING SUPPORT PILLOW PREMIUM
Catalogue references include 004, 030/17, 032/17, 033/17, 034/17, 036.
European nomenclature codes declared: T04010202, V080302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. Motherhood Sp. z o.o. was not found in either the U.S. or the Canadian register.