- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 30, 2026
69713904306068C3 references
69713904306068CHOK-CE-BETA2-MG-CPSR-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 →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.
W0102039002Beta2-microglobulin3 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 |
|---|---|---|---|---|---|
| HOKAPI™ BETA2-MG | HOKAPI™ BETA2-MG | 010606601 | 06939716405127 | 100 | On the market |
| HOKAPI™ BETA2-MG | HOKAPI™ BETA2-MG | 010606101 | 06971390439890 | 100 | On the market |
| HOKAPI™ BETA2-MG | HOKAPI™ BETA2-MG | 010606001 | 06939716405110 | 50 | On the market |