Mustaf Medical Spółka cywilna Anna Kowalska Rafał Kowalski
PL-MF-000032664 · Poland · Łobodno
Mustaf Medical Spółka cywilna Anna Kowalska Rafał Kowalski is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 35 |
|---|
Devices declared under this manufacturer
- CareProx Pure
- Careprox Light, 39x50 cm, 50 mb
- Careprox Light, 50x50 cm, 40 mb
- Careprox Light, 50x50 cm, 50 mb
- Careprox Light, 60x50 cm, 40 mb
- Careprox Light, 60x50 cm, 50 mb
- Careprox Protect, 30x50 cm, 20 mb
- Careprox Protect, 33x50 cm, 20 mb
Showing 12 of 35 declared devices.
Catalogue references include POCL B 39/50/50, POCL N 39/50/50, POCL N 50/50/40, POCL N 60/50/50, POCP N, POCP Z.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| 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 | 35 |
|---|---|
| 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. Mustaf Medical Spółka cywilna Anna Kowalska Rafał Kowalski was not found in either the U.S. or the Canadian register.