Sidam S.R.L.
IT-MF-000030697 · Italy · Mirandola
Sidam S.R.L. is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Among these devices, 8 are declared sterile.
Catalogue references include 01011002, 021-400, 022-122, 022-500, 24A1A00007, 4010-S.
European nomenclature codes declared: A03040199, A03020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | SIDAM S.R.L. |
What it holds in Canada
| Licences on record | 3 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 3 |
| First licensed | 2010-08-10 |
Licence types: Device Group Family (3).
Licensed under: "MUST KIT" - MULTI-USE TUBING KIT, ENTERAL FEEDING TUBE "NUTRIVENT", MUST KIT PLUS.
North American profile: Canada only. Sidam S.R.L. holds a Canadian licence but was not found in the U.S. register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
ITH 2423536 1 | issued | 2029-03-17 |
ITD 2423536 1 | supplemented | 2029-03-17 |