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Hokapi™ Ca 242

EUDAMED

Class C (EU MDR)

Ref 010109601Ref 010109001Ref 010109101

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ CA 242 EUDAMED
Device Name
HOKAPI™ CA 242 EUDAMED
Model / Reference
010109601 EUDAMED
010109001 EUDAMED
010109101 EUDAMED

Identifiers

Primary DI / UDI-DI
06939716404540 EUDAMED
06939716404533 EUDAMED
06971390439654 EUDAMED
Basic UDI-DI
69713904301097R EUDAMED
Direct Marketing DI
06939716404540 EUDAMED
06939716404533 EUDAMED
06971390439654 EUDAMED
EMDN Code
W0102030108 CANCER ANTIGEN 242 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™ Ca 242 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 (3)

  • EUDAMED fd929360-2d66-4918-a0e4-69348058f460 61 fields · synced Jul 22, 2026
  • EUDAMED 4fdea9fd-3020-4942-963e-bc3b7b87efba 61 fields · synced May 18, 2026
  • EUDAMED 356c4094-6af4-4a70-85a1-01880380c0ba 61 fields · synced May 19, 2026