Contipro a.s.
CZ-MF-000014702 · Czechia · Dolní Dobrouč
Contipro a.s. is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 9 |
|---|
Most frequent device types declared: Hyatoprol 22g, Sorelex 10x10 (10pcs), 35 mg, Hyatoprol 50g, Hyiodine 22g.
Among these devices, 9 are declared sterile, 1 implantable.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Czechia |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
2026-MDR/TD-031 | issued | 2028-08-04 |
2026-MDR/QS-031 | issued | 2028-08-04 |
2025-MDR/TD-033 | issued | 2028-08-04 |
2025-MDR/QS-033 | issued | 2028-08-04 |
2023-MDR/TD-016 | issued | 2028-08-04 |
2023-MDR/QS-016 | issued | 2028-08-04 |