Know Medical Srl
IT-MF-000013457 · Italy · Viadana
Know Medical Srl is registered in the European database on medical devices as a manufacturer, with 317 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 317 |
|---|
Most frequent device types declared: SERODRAIN - Sacca priming 2000 ml con LLF.
Among these devices, 317 are declared sterile, 11 active.
Devices declared under this manufacturer
- BURETTE
- DOSIKNOW
- ENTINFUSION
- EXTENSION LINE
- HUBER NEEDLE
- INFUSET
- ONCOFUX
- PAR INFUSION
- PARINFUSION
- SERODRAIN
- TRANSFUSET
- URINE BAG
Showing 12 of 317 declared devices.
Catalogue references include EL075117-O, EL090230-O, EL100005-O, FL2 132 O, PB015000-O, PB200300-O.
European nomenclature codes declared: A03020101, A0799, A080102, A0601010103, A03010101, A06030301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 317 |
| 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 | 222 |
|---|---|
| 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. Know Medical Srl was not found in either the U.S. or the Canadian register.