- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 30, 2026
69713904304027S4 references
69713904304027SHOK-CE-LH-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.
W0102050105Luteinising hormone4 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™ LH | HOKAPI™ LH | 010402601 | 06939716404922 | 100 | On the market |
| HOKAPI™ LH | HOKAPI™ LH | 010402401 | 06971390434918 | 50 | On the market |
| HOKAPI™ LH | HOKAPI™ LH | 010402101 | 06971390434925 | 100 | On the market |
| HOKAPI™ LH | HOKAPI™ LH | 010402001 | 06939716404915 | 50 | On the market |