Copratex srl
IT-MF-000029674 · Italy · Prato
Copratex srl is registered in the European database on medical devices as a manufacturer, with 379 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 379 |
|---|
Most frequent device types declared: CAMICE, CAMICE MICROFIBRA/LAMINATO TG.L.
Among these devices, 282 are declared reusable.
Devices declared under this manufacturer
- CHTG-XXXLCZ670V
- CSTG-UCIG019LSG
- CSTG-UCSIV
- CSTG-UCZ595BISG
- STM095X150CZV
- TELO ANGIOGRAFICO HIGH PERFORMANCE
- TH 170X180BRNA
- TH050X230CZ774RBL
- TH090X090CZ724V
- TH090X140CZ125V
- TS040X050CZ711V
- TS040X100CGTE039V
Showing 12 of 379 declared devices.
Catalogue references include 106, 118, 152, 181, 285, 359.
European nomenclature codes declared: T020199, T020401.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 379 |
| 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 | 379 |
|---|---|
| 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. Copratex srl was not found in either the U.S. or the Canadian register.