Inpeco SA
CH-MF-000017833 · Switzerland · Novazzano
Inpeco SA is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: FPB, PTB, TLA.
Authorised representative in the Union: QbD RepS BV.
Devices declared under this manufacturer
- Accelerator a3600
- Aptio® Automation
- FlexLab
- FlexLab X
- FlexPath Blox
- ProTube
Catalogue references include ACP, AP2, FLX, FPB, FXX, PTB.
European nomenclature codes declared: W02060101, W0202059099, W0202059004, W0299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | INPECO SA (CH) · FDA 3010825766 |
| Devices in EUDAMED | 7 |
| Country of registration | Switzerland |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| Found in the U.S. device database | 6 |
| Share | 85.7 % |
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: United States only. Inpeco SA is registered in the United States but was not found in the Canadian register.