KIRMED INTERNATIONAL SRL
IT-MF-000035071 · Italy · Camposampiero (PD)
KIRMED INTERNATIONAL SRL is registered in the European database on medical devices as a manufacturer, with 110 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 89 |
|---|---|
| Class IIb | 21 |
Most frequent device types declared: Punte pluriuso, Punte monouso sterili, Manipolo per K-Bisonic/K-Sonic, K-Sonic, K-Bisonic.
Among these devices, 38 are declared sterile, 67 reusable, 21 active.
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 | 110 |
| Country of registration | Italy |
⚠️ 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.