MOSS S.p.A.
IT-MF-000010071 · Italy · LESA
MOSS S.p.A. is registered in the European database on medical devices as a manufacturer, with 90 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 90 |
|---|
Devices declared under this manufacturer
- NOVOX 5mL-10 pcs.
- NOVOX ANDRO L.10 cm d.2 cm 1pc.
- NOVOX ANDRO L.12 cm d.3 cm 1pc.
- NOVOX CUP MINI PIN 2pcs.
- NOVOX CUP XL 2pcs.
- NOVOX DROP 5mL-1pc.
- NOVOX FIT 10x10cm-16 la. - 10 pcs.
- NOVOX GYNO - 15 ml
- NOVOX ROLL 4,5mx8cm - 10 pcs.
- NOVOX SLIM 5m x 2cm - 10pcs
- NOVOX SLIM 5mx2cm - 10 pcs.
- NOVOX TOUCH L 1 pc.
Showing 12 of 90 declared devices.
Catalogue references include NGT015S-SL, NMA-L12D03-1, NS005, NS005-L2, NSL5x2, NSL5x2-L2.
European nomenclature codes declared: M040413, U0803.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 90 |
| 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 | 90 |
|---|---|
| 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. MOSS S.p.A. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
EPT 0477.MDR.22/4952 | issued | 2027-10-06 |
EPT 0477.MDR.22/4951 | issued | 2027-10-06 |