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Hokapi™ Myoglobin

EUDAMED

Class C (EU MDR)

Ref 010702001

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ MYOGLOBIN EUDAMED
Device Name
HOKAPI™ MYOGLOBIN EUDAMED
Model / Reference
010702001 EUDAMED

Identifiers

Primary DI / UDI-DI
06939716405134 EUDAMED
Basic UDI-DI
697139043070289 EUDAMED
Direct Marketing DI
06939716405134 EUDAMED
EMDN Code
W01021304 MYOGLOBIN 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™ Myoglobin 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 (1)

  • EUDAMED 4c9432d8-abe5-4456-bc68-56fea7b474c0 61 fields · synced Jun 19, 2026