Identity
- Trade Name
- HOKAPI™ PROGRP EUDAMED
- Device Name
- HOKAPI™ PROGRP EUDAMED
- Model / Reference
- 010122001 EUDAMED010122601 EUDAMED010122101 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06939716404694 EUDAMED06939716404700 EUDAMED06971390439739 EUDAMED
- Basic UDI-DI
- 69713904301227H EUDAMED
- Direct Marketing DI
- 06939716404694 EUDAMED06939716404700 EUDAMED06971390439739 EUDAMED
- EMDN Code
- W0102030121 PRO-GASTRIN-RELEASING PEPTIDE EUDAMED
Classification
- Device Class
- Class C EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Hokapi™ Progrp by Suzhou Hokapi Biomedical Engineering Co., Ltd.. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 69713904301227H | Class C | Active |
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Manufacturer
- Manufacturer
- Suzhou Hokapi Biomedical Engineering Co., Ltd..
- EUDAMED SRN
- CN-MF-000013723
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (3)
- EUDAMED 64a792f5-eb13-4000-be5b-a2371b16f2ae 61 fields · synced Jul 11, 2026
- EUDAMED e7f52215-15cb-4b96-a80b-54ffb7947fc9 61 fields · synced May 17, 2026
- EUDAMED 938e131e-0639-4ac0-b0c2-4a0666939a9b 61 fields · synced May 19, 2026