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Urıc Acid Kit

EUDAMED

Class IVD General (EU MDR)

Ref B21296Model Uric Acid Kit 240mL

by Ki̇neti̇k Bi̇li̇şi̇m Di̇agnosti̇k Anoni̇m Şi̇rketi̇

Identity

Trade Name: Urıc Acid Kit EUDAMED
Device Name: Uric Acid Kit EUDAMED
Model / Reference: Uric Acid Kit 240mL EUDAMED
B21296 EUDAMED

Identifiers

Primary DI / UDI-DI: 08683555611048 EUDAMED
Basic UDI-DI: B-08683555611048 EUDAMED
EMDN Code: W01010232 URIC ACID EUDAMED

Classification

Device Class: Class IVD General EUDAMED
Market of Registration: Türkiye 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

Category: Uric acid IVD, reagent

Urıc Acid Kit by Ki̇neti̇k Bi̇li̇şi̇m Di̇agnosti̇k Anoni̇m Şi̇rketi̇ — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Uric acid IVD, reagent.

URIC ACID REAGENT KIT（URICASE METHOD） — DIRUI INDUSTRIAL CO., LTD · IVD General
BIOBASE — Biobase Biodustry(Shandong)Co., Ltd. · Class I
Uric Acid (UA) — Maccura Biotechnology Co., Ltd. · IVD General
Liquick Cor-UA 120 — PZ CORMAY Spółka Akcyjna · IVD General
BIOBASE — Biobase Biodustry(Shandong)Co., Ltd. · Class I
JAS Diagnostics — Drew Scientific , Ltd. · Class I
Uric acid — Kalians Corporation · IVD General
ACE — Alfa Wassermann, Inc. · Class I

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer: Ki̇neti̇k Bi̇li̇şi̇m Di̇agnosti̇k Anoni̇m Şi̇rketi̇
EUDAMED SRN: TR-MF-000040334

Sources (1)

EUDAMED 6ae2c45f-7f15-4d48-91f0-d367a234798d 61 fields · synced Jun 18, 2026