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Hokapi™ Scc

EUDAMED

Class C (EU MDR)

Ref 010113001Ref 010113601

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ SCC EUDAMED
Device Name
HOKAPI™ SCC EUDAMED
Model / Reference
010113001 EUDAMED
010113601 EUDAMED

Identifiers

Primary DI / UDI-DI
06939716404618 EUDAMED
06939716404625 EUDAMED
Basic UDI-DI
69713904301137G EUDAMED
Direct Marketing DI
06939716404618 EUDAMED
06939716404625 EUDAMED
EMDN Code
W0102030116 SQUAMOUS CELL CARCINOMA ANTIGEN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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™ Scc 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

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Manufacturer

EUDAMED SRN
CN-MF-000013723
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED 0f79ed2f-4835-4df3-89c7-43c47757e29e 61 fields · synced Aug 3, 2026
  • EUDAMED e6049a07-4aa1-4b00-ac09-556c639c2ca6 61 fields · synced May 18, 2026