Ebizlab srl
IT-MF-000046729 · Italy · Cosenza
Ebizlab srl is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: CARROZZINA AD AUTOSPINTA MOD. B, CARROZZINA AD AUTOSPINTA MOD.A, ROLLATOR.
Devices declared under this manufacturer
- CARROZZINA AD AUTOSPINTA MOD. A
- CARROZZINA AD AUTOSPINTA MOD. B
- ROLLATOR DEAMBULATORE PIEGHEVOLE
- ROLLATOR DEAMBULATORE PIEGHEVOLE B
Catalogue references include 28996, 31671, 31672, 37135, MK350 (26283-29350), MK351 (26283-29351).
European nomenclature codes declared: Y122106, Y120609.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. Ebizlab srl was not found in either the U.S. or the Canadian register.