MTD Diagnostics srl
IT-MF-000053242 · Italy · San Marco Evangelista
MTD Diagnostics srl is registered in the European database on medical devices as a manufacturer, with 106 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Albumin-BCG LS Mono
- Amylase CNPG3 LS Mono
- Bilirubin T+D DPD LS
- CLIA Wash Buffer
- Diluent 3 Diff H3
- Homocysteine LS HP
- Kappa Light Chain Antibody + Cal/Cont
- LDH-L LS
- Lipase LS
- Lyse 3 Diff H3
- RF Latex Slide
- Rinse 5 Diff H5
Showing 12 of 106 declared devices.
Catalogue references include AC1010; ITAC1010, CC1002 - CC1003, CC1038, CC1256; CC1257, M3001; M3000, M3003; M3006.
European nomenclature codes declared: W0103010105, W01019099, W01010203, W01021110, W0101060299, W01010207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 106 |
| 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 | 29 |
|---|---|
| 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. MTD Diagnostics srl was not found in either the U.S. or the Canadian register.