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: K-Bisonic, K-Sonic, Manipolo per K-Bisonic/K-Sonic, Punte monouso sterili, Punte pluriuso.
Among these devices, 38 are declared sterile, 67 reusable, 21 active.
Devices declared under this manufacturer
- Console sistema elettromedicale K-Bisonic Spino
- Console sistema elettromedicale K-Bisonic2
- Console sistema elettromedicale K-Sonic Dental
- Console sistema elettromedicale K-Sonic I.Son
- Console sistema elettromedicale K-Sonic2
- Manipolo 27 kHz per K-Bisonic/K-Sonic
- Manipolo 35 kHz per K-Bisonic/K-Sonic
- Manipolo 50 kHz per K-Bisonic/K-Sonic
- Punta uso esclusivo a 27 kHz
- Punta uso esclusivo a 35 kHz
- Punta uso esclusivo a 50 kHz
Showing 12 of 110 declared devices.
Catalogue references include K706M, K718, K719, K722, K725, K732M.
European nomenclature codes declared: Z12010885, Z12010801.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 110 |
| 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 | 110 |
|---|---|
| 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. KIRMED INTERNATIONAL SRL was not found in either the U.S. or the Canadian register.