Maximus s.c. Robert Klejdysz, Alicja Daniecka-Klejdysz
PL-MF-000045281 · Poland · Szczecin
Maximus s.c. Robert Klejdysz, Alicja Daniecka-Klejdysz is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 |
|---|
Among these devices, 1 are declared reusable, 6 active.
Devices declared under this manufacturer
- Komora kriogeniczna AMAZING MX-4CP
Catalogue references include BLUE AIR MX-2, BLUE LINE, CARGO MX-3, Sani MX-O3, Tower MX-1, wersja męska lub damska.
European nomenclature codes declared: Z12069003, V9099, V0899, M9001, R0699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| 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. Maximus s.c. Robert Klejdysz, Alicja Daniecka-Klejdysz was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1434-MDR-023/2024 | issued | 2030-01-08 |