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UPROTEIN Kit

EUDAMED

Class IVD General (EU MDR)

Ref B21303Model UPROTEIN KitRef B21304

by Ki̇neti̇k Bi̇li̇şi̇m Di̇agnosti̇k Anoni̇m Şi̇rketi̇

Identity

Trade Name
UPROTEIN Kit EUDAMED
Device Name
UPROTEIN Kit EUDAMED
Model / Reference
UPROTEIN Kit EUDAMED
B21303 EUDAMED
B21304 EUDAMED

Identifiers

Primary DI / UDI-DI
08683555625366 EUDAMED
08683555625373 EUDAMED
Basic UDI-DI
B-08683555625366 EUDAMED
B-08683555625373 EUDAMED
EMDN Code
W0101060106 UREA TEST STRIPS 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

UPROTEIN Kit by Ki̇neti̇k Bi̇li̇şi̇m Di̇agnosti̇k Anoni̇m Şi̇rketi̇ — 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
TR-MF-000040334

Sources (2)

  • EUDAMED a2bdc029-7768-4bee-ac79-f2f82ecc5a05 61 fields · synced Oct 6, 2026
  • EUDAMED 64cde866-8d18-4490-8cb2-70fd101baeb8 61 fields · synced May 17, 2026