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Hokapi™ Substrate Solution 2

EUDAMED

Class A (EU MDR)

Ref 010913301Ref 010912301

by Suzhou Hokapi Biomedical Engineering Co., Ltd..

Identity

Trade Name
HOKAPI™ SUBSTRATE SOLUTION 2 EUDAMED
HOKAPI™ SUBSTRATE SOLUTION 1 EUDAMED
Device Name
HOKAPI™ SUBSTRATE SOLUTION 2 EUDAMED
HOKAPI™ SUBSTRATE SOLUTION 1 EUDAMED
Model / Reference
010913301 EUDAMED
010912301 EUDAMED

Identifiers

Primary DI / UDI-DI
06971390435014 EUDAMED
06971390435007 EUDAMED
Basic UDI-DI
69713904309138Q EUDAMED
69713904309128N EUDAMED
Direct Marketing DI
06971390435014 EUDAMED
06971390435007 EUDAMED
EMDN Code
W0201020185 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - CONSUMABLES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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™ Substrate Solution 2 by Suzhou Hokapi Biomedical Engineering Co., Ltd.. — Class A — 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 4dc3bc3b-db22-4d28-b6b5-56948029a8e6 61 fields · synced Jul 23, 2026
  • EUDAMED c9c64974-a229-49dd-af3f-0f316acc1db2 61 fields · synced May 19, 2026