AB ANALITICA srl
IT-MF-000032625 · Italy · Padova
AB ANALITICA 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 | 3 |
|---|
Most frequent device types declared: BREATH BAG IN ALLUMINIO, CANNUCCE PER L'ESECUZIONE DEL TEST DEL RESPIRO.
Devices declared under this manufacturer
- BREATH BAG IN ALLUMINIO
- GENEQUALITY 2050
- GENEQUALITY 2050 Extraction C
- GENEQUALITY 2050 Extraction P
Catalogue references include 05-25C-3A, 05-25P-3A, 08-GQ2050-01, 15-21-001, 15-21-100 CT, 15-26-100.
European nomenclature codes declared: W0105900101, A99, V80, W02050116.
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. AB ANALITICA srl was not found in either the U.S. or the Canadian register.