Reflexx
IT-MF-000021631 · Italy · VIADANA
Reflexx is registered in the European database on medical devices as a manufacturer, with 126 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 126 |
|---|
Devices declared under this manufacturer
- PRODONTO ABT GLOVES SIGNATURE SERIES - SIZE L
- REFLEXX 44 BLACK - SIZE L
- REFLEXX 68 - SIZE XL
- REFLEXX 72 - SIZE L
- REFLEXX 72 - SIZE S
- REFLEXX 77 - SIZE M
- REFLEXX 78 BLACK - SIZE M
- REFLEXX 78 BLACK - SIZE S
- REFLEXX 99 NHR - SIZE M
- REFLEXX 99 NHR - SIZE S
- REFLEXX CARE N350 - SIZE L
- REFLEXX N100 - SIZE M
Showing 12 of 126 declared devices.
Catalogue references include N69/S, N82/S, R44/L, R72/L, R78/M, R78/S.
European nomenclature codes declared: T01020204, T010201, T01020201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 126 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 126 |
|---|---|
| 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. Reflexx was not found in either the U.S. or the Canadian register.