- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Aug 26, 2026
5060520350426DF7Q5 references
5060520350426DF7QBasic 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.
L031302Medication forceps, reusableL03130403Splinter forceps, reusable5 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 |
|---|---|---|---|---|---|
| Surgimax | Surgimax | 05-130-11 | 05060520352503 | 1 | On the market |
| Surgimax | Surgimax | 05-135-08 | 05060520352497 | 1 | On the market |
| Surgimax | Surgimax | 05-901-08 | 05060520352473 | 1 | On the market |
| Surgimax | Surgimax | 05-130-01 | 05060520352510 | 1 | On the market |
| Surgimax | Surgimax | 05-136-10 | 05060520352480 | 1 | On the market |