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Glucose Kit(Hexokinase Method)

EUDAMED

Class IVD General (EU MDR)

Ref 5632Model "R1:2x60ml R2:2x15ml "

by Coei Biotech Co.Ltd.

Identity

Trade Name
Glucose Kit(Hexokinase Method) EUDAMED
Device Name
Glucose Kit(Hexokinase Method) EUDAMED
Model / Reference
"R1:2x60ml R2:2x15ml " EUDAMED
5632 EUDAMED

Identifiers

Primary DI / UDI-DI
06977565585638 EUDAMED
Basic UDI-DI
B-06977565585638 EUDAMED
EMDN Code
W01010213 GLUCOSE EUDAMED

Classification

Device Class
Class IVD General 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

Glucose Kit(Hexokinase Method) by Coei Biotech Co.Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000049509
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 3881b46f-45cd-4ba1-b347-226f0a84fb0d 61 fields · synced Jun 20, 2026