- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 8, 2026
80540851218P25 references
80540851218P2No device characteristics flagged
0425-MDR-030119-01Basic 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 →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
Q0299Ophthalmic devices - other5 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 |
|---|---|---|---|---|---|
| Contact Care Drops Plus (GOEC-005) | Contact Care Drops Plus (GOEC-005) | 050596 | 08054085122272 | 1 | On the market |
| Ektal M (GOEC-003) | Ektal M (GOEC-003) | 050550 | 08054085122142 | 1 | On the market |
| Ektal M (GOECP-004) | Ektal M (GOECP-004) | 050639 | 08054085122500 | 1 | On the market |
| Protection Eye Drop (GOECP-002) | Protection Eye Drop (GOECP-002) | 050615 | 08054085122210 | 1 | On the market |
| Reflex Gocce oculari (GOEC-002) | Reflex Gocce oculari (GOEC-002) | 050483 | 08054085121800 | 1 | On the market |