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Hokapi™ Psa

EUDAMED

Class C (EU MDR)

Ref 010103601Ref 010103101Ref 010103001

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ PSA EUDAMED
Device Name
HOKAPI™ PSA EUDAMED
Model / Reference
010103601 EUDAMED
010103101 EUDAMED
010103001 EUDAMED

Identifiers

Primary DI / UDI-DI
06939716404427 EUDAMED
06971390434987 EUDAMED
06939716404410 EUDAMED
Basic UDI-DI
69713904301037D EUDAMED
Direct Marketing DI
06939716404427 EUDAMED
06971390434987 EUDAMED
06939716404410 EUDAMED
EMDN Code
W0102030113 TOTAL PROSTATIC SPECIFIC 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™ Psa 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 7177e2e3-e882-4e11-bef3-3687c1ef9b8a 61 fields · synced Jul 28, 2026
  • EUDAMED 6308bfe6-c9ec-4b86-8eb3-eb8fcfd0b7b5 61 fields · synced May 17, 2026
  • EUDAMED d75411ce-ec3f-4ab0-b771-eda72f5c6eed 61 fields · synced May 19, 2026