NEULABS S.R.L.
IT-MF-000052932 · Italy · Milano
NEULABS S.R.L. is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|
Most frequent device types declared: TOPPER ALOE DOLCISOGNI.
Devices declared under this manufacturer
- ALOE TOP 100x190x5
- ALOE TOP 110x190x5
- ALOE TOP 120X190X7
- ALOE TOP 120x190x3
- ALOE TOP 120x200x5
- ALOE TOP 140X190X7
- ALOE TOP 140X200X5
- ALOE TOP 160X190X7
- ALOE TOP 180x200x7
- ALOE TOP 80X190X5
- ALOE TOP 80x190x3
- ALOE TOP 90X190X5
Showing 12 of 29 declared devices.
Catalogue references include TOP_100x190x5_ALOE, TOP_110x190x5_ALOE, TOP_120X190X7_ALOE, TOP_120x190x3_ALOE, TOP_120x200x5_ALOE, TOP_160X190X7_ALOE.
European nomenclature codes declared: V080702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| 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 | 29 |
|---|---|
| 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. NEULABS S.R.L. was not found in either the U.S. or the Canadian register.