- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jun 19, 2026
69713904301227H3 references
69713904301227HHOK-CE-PROGRP-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.
W0102030121Pro-gastrin-releasing peptide3 references
| Product | Trade name | Reference / catalog number | UDI-DI code | Quantity | Status |
|---|---|---|---|---|---|
| HOKAPI™ PROGRP | HOKAPI™ PROGRP | 010122101 | 06971390439739 | 100 | On the market |
| HOKAPI™ PROGRP | HOKAPI™ PROGRP | 010122601 | 06939716404700 | 100 | On the market |
| HOKAPI™ PROGRP | HOKAPI™ PROGRP | 010122001 | 06939716404694 | 50 | On the market |