DAS Srl
IT-MF-000035583 · Italy · Palombara Sabina (Roma)
DAS Srl is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- ACTION
- AP-BLOT ELITE
- AP16 IF BLOT ELITE
- AP16 IF ELITE
- AP22 ELITE
- AP22 IF BLOT ELITE
- AP22 IF ELITE
- AP32 IF ELITE
- APE ELITE
- APE IF ELITE
- BLOT MODULE
- HB ANALYZER Plus
Showing 12 of 14 declared devices.
Catalogue references include OR-0600, OR-102402, OR-102403, OR-105401, OR-1166011, OR-123201.
European nomenclature codes declared: W0201020102, W0201020201, W0201020180, W0201020182, W02010199, W02010299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| 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 | 14 |
|---|---|
| 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. DAS Srl was not found in either the U.S. or the Canadian register.