Data from EUDAMED, last updated Jul 31, 2026
69713904301167N3 references
69713904301167NHOK-CE-PG II-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.
W0102069006Pepsinogen3 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™ PG II | HOKAPI™ PG II | 010116001 | 06939716404670 | 50 | On the market |
| HOKAPI™ PG II | HOKAPI™ PG II | 010116601 | 06939716404687 | 100 | On the market |
| HOKAPI™ PG II | HOKAPI™ PG II | 010116101 | 06971390439722 | 100 | On the market |