BRENTA S.R.L.
IT-MF-000012490 · Italy · Camponogara
BRENTA S.R.L. is registered in the European database on medical devices as a manufacturer, with 279 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 279 |
|---|
Most frequent device types declared: Copriscarpe, Guanto in Lattice da Esaminazione, Guanto in Nitrile da Esaminazione, Guanto in Vinile da Esaminazione, Mascherine Chirurgiche.
Devices declared under this manufacturer
- Automat Easy walking
- Bioderm Walking
- Lavender Walking
- Nitrile Nero Guadagnopack
- Nitrile Nero Maurer Plus
- Nitroflex Walking
- Nitrofort 8 Arancio Grip Walking
- Nitrogel Blu Walking
- Nitrogel Nero Walking
- Nitromax Long Nero Walking
- Nitromax Long Walking
- Nitrox Nero Walking
Showing 12 of 279 declared devices.
Catalogue references include 010268, 011787, 012252, 012383, 012683, 016861.
European nomenclature codes declared: T01020204, T010201, T01020201, T0208, T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 279 |
| 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 | 279 |
|---|---|
| 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. BRENTA S.R.L. was not found in either the U.S. or the Canadian register.