- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
76300039MD010516TB3 references
76300039MD010516TBNo device characteristics flagged
Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
Q020402Posterior vitrectomy sets3 references
| Product | Trade name | Reference / catalog number | Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary → | Quantity | Status |
|---|---|---|---|---|---|
| Vitrectomy pack Faros 23G | Vitrectomy pack Faros 23G | VV621213BP | 07630003912951 | 1 | On the market |
| Vitrectomy pack Faros 25G | Vitrectomy pack Faros 25G | VV621215BP | 07630003912968 | 1 | On the market |
| Vitrectomy pack Faros 27G | Vitrectomy pack Faros 27G | VV621217BP | 07630003915631 | 1 | On the market |