PERIDENT DENTAL PRODUCTS s.r.l.
IT-MF-000044166 · Italy · Bagno a Ripoli (FI)
PERIDENT DENTAL PRODUCTS s.r.l. is registered in the European database on medical devices as a manufacturer, with 108 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 108 |
|---|
Devices declared under this manufacturer
- PRODONTO CUNEI INTERDENTALI IN LEGNO
- WESTPOINT CLAMP-MAT MATRICI ACCIAIO
- WESTPOINT CUNEI INTERDENTALI IN LEGNO
- WESTPOINT CUNEI INTERDENTALI TRASPARENTI
- WESTPOINT KITE PINZA PER MATRICI
- WESTPOINT MATRICI A NASTRO ACCIAIO
- WESTPOINT MATRICI A NASTRO POLIESTERE TRASPARENTE
- WESTPOINT MATRICI ADESIVE TRASPARENTI
- WESTPOINT SMS ANELLO STANDARD DI FISSAGGIO PER MATRICI SEZIONALI
- WESTPOINT SMS MATRICI SEZIONALI ACCIAIO
- WESTPOINT SMS MATRICI SEZIONALI ACCIAIO DOPPIA CURVA
- WESTPOINT SMS MATRICI SEZIONALI TITANIO
Showing 12 of 108 declared devices.
Catalogue references include 3505, 3506, 3530, 3620, 3716, 3930.
European nomenclature codes declared: Q01010401, Q010199, Q01010403, Q0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 108 |
| 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 | 108 |
|---|---|
| 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. PERIDENT DENTAL PRODUCTS s.r.l. was not found in either the U.S. or the Canadian register.