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Uric Acid Reagent Kit(uricase Method)

EUDAMED

Class IVD General (EU MDR)

Ref 3019372Model R1: 2L, R2: 500mL,Calibration sample: 20mL

by Dirui Industrial Co., Ltd

Identity

Trade Name
URIC ACID REAGENT KIT(URICASE METHOD) EUDAMED
Device Name
URIC ACID REAGENT KIT(URICASE METHOD) EUDAMED
Model / Reference
R1: 2L, R2: 500mL,Calibration sample: 20mL EUDAMED
3019372 EUDAMED

Identifiers

Primary DI / UDI-DI
06925794581211 EUDAMED
Basic UDI-DI
B-06925794581211 EUDAMED
EMDN Code
W01010232 URIC ACID EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

Yes

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 Reagent Kit(uricase Method) by Dirui Industrial 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-000001891
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED b566cd59-50b4-42f7-9818-bbabccfb8e4d 61 fields · synced Jun 20, 2026