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Hokapi™ Cea

EUDAMED

Class C (EU MDR)

Ref 010101001Ref 010101601

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ CEA EUDAMED
Device Name
HOKAPI™ CEA EUDAMED
Model / Reference
010101001 EUDAMED
010101601 EUDAMED

Identifiers

Primary DI / UDI-DI
06939716404373 EUDAMED
06939716404380 EUDAMED
Basic UDI-DI
697139043010179 EUDAMED
Direct Marketing DI
06939716404373 EUDAMED
06939716404380 EUDAMED
EMDN Code
W0102030112 CARCINOEMBRYONIC 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™ Cea 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 1e31110d-f5e8-4a89-b54c-1cb8ba929d58 61 fields · synced Jul 11, 2026
  • EUDAMED c6736d8c-c96a-4f1f-a006-e6b4f9b248e3 61 fields · synced May 19, 2026