Nano-Tech Polska Sp. z o.o. Sp. Kom.
PL-MF-000010978 · Poland · Warszawa
Nano-Tech Polska Sp. z o.o. Sp. Kom. is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 19 |
|---|
Devices declared under this manufacturer
- Nanobiotic MED Dziąsła i Afty
- Nanobiotic MED Gold Regeneracja
- Nanobiotic MED Intima
- Nanobiotic MED Silver Gardło
- Nanobiotic MED Silver Katar
- Nanobiotic MED Silver Nase und Nebenhöhlen
- Nanobiotic MED Silver Plus Forte
- Nanobiotic MED Silver Rachen
- axoCare Pianka na Odparzenia
- axoCare Pianka na Oparzenia, Podrażnienia i Stany Zapalen Skóry
- axobiotic Gardło
- axobiotic Gardło Kids 2w1
Showing 12 of 19 declared devices.
Catalogue references include GERMEDNASE, MEDABGAR, MEDABKK, MEDDIA, MEDFOR, MEDINT300.
European nomenclature codes declared: V9099, Q030199, V9017.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| 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 | 19 |
|---|---|
| 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. Nano-Tech Polska Sp. z o.o. Sp. Kom. was not found in either the U.S. or the Canadian register.