FARMA-DERMA S.r.l.
IT-MF-000020737 · Italy · SALA BOLOGNESE (BOLOGNA)
FARMA-DERMA S.r.l. is registered in the European database on medical devices as a manufacturer, with 124 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 120 |
|---|---|
| Class IIa | 4 |
Devices declared under this manufacturer
- CICATRIDINA mast
- CICATRIDINA ovules vaginaux
- CICATRIDINA spray
- CICATRIDINA маз
- CICATRIDINA супозитории
- HEMOREINE suppositoires
- IALOCLEAN SPRAY NASALE
- IALOCLEAN SPRAY PER MUCOSA ORO-FARINGEA
- PROKTIS-M PLUS mast za rektum
- PROKTIS-M czopki
- PROKTIS-M čepići
- REPADINA PLUS vagitorier
Showing 12 of 124 declared devices.
Catalogue references include 1029, 1035, 1047, 1105, 2018, 2020.
European nomenclature codes declared: M040499, G05, U0803, Q0399.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | FARMA-DERMA S.R.L. (IT) · FDA 3013474580 |
| Devices in EUDAMED | 124 |
| Country of registration | Italy |
Device-level evidence
| Devices with a numeric GTIN | 124 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | FARMA-DERMA S.R.L. |
North American profile: Both markets. FARMA-DERMA S.r.l. is registered in both the United States and Canada.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
EPT 0477.MDR.25/5818 | issued | 2027-12-19 |
EPT 0477.MDR.25/5817 | issued | 2027-12-19 |
EPT 0477.MDR.23/5102.1 | reissued | 2027-12-19 |
EPT 0477.MDR.23/5032.1 | reissued | 2027-12-19 |
EPT 0477.MDR.22/5022 | issued | 2027-12-19 |
EPT 0477.MDR.22/5021 | issued | 2027-12-19 |
EPT 0477.MDR.22/5020 | issued | 2027-12-19 |
EPT 0477.MDR.22/5019 | issued | 2027-12-19 |