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Hokapi™ Insulin

EUDAMED

Class C (EU MDR)

Ref 010601601Ref 010601101

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ INSULIN EUDAMED
Device Name
HOKAPI™ INSULIN EUDAMED
Model / Reference
010601601 EUDAMED
010601101 EUDAMED

Identifiers

Primary DI / UDI-DI
06939716405080 EUDAMED
06971390439876 EUDAMED
Basic UDI-DI
697139043060182 EUDAMED
Direct Marketing DI
06939716405080 EUDAMED
06971390439876 EUDAMED
EMDN Code
W0102060103 INSULIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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™ Insulin 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 fa14c979-dccb-4b19-b254-ed61c07719de 61 fields · synced Jul 23, 2026
  • EUDAMED b1333eb9-20d3-4174-8ecb-0b4d34100c4f 61 fields · synced May 16, 2026