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Uric Acid Kit( Uricase Method)

EUDAMED

Class IVD General (EU MDR)

Ref 4932Model "R1:2x60ml R2:2x15ml "

by Coei Biotech Co.Ltd.

Identity

Trade Name
Uric Acid Kit( Uricase Method) EUDAMED
Device Name
Uric Acid Kit( Uricase Method) EUDAMED
Model / Reference
"R1:2x60ml R2:2x15ml " EUDAMED
4932 EUDAMED

Identifiers

Primary DI / UDI-DI
06977565584938 EUDAMED
Basic UDI-DI
B-06977565584938 EUDAMED
EMDN Code
W01010232 URIC ACID 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

Category: Uric acid IVD, reagent

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

Similar devices

Also classified as Uric acid IVD, reagent.

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 4b0b20ea-496d-4517-a893-eed0a5f0db88 61 fields · synced Jul 9, 2026