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A-800 Ua

EUDAMED

Class IVD General (EU MDR)

Ref 7-813Model A-800 UA

by PZ CORMAY Spółka Akcyjna

Identity

Trade Name
A-800 UA EUDAMED
Device Name
UA EUDAMED
Model / Reference
A-800 UA EUDAMED
7-813 EUDAMED

Identifiers

Primary DI / UDI-DI
05907514678136 EUDAMED
Basic UDI-DI
B-05907514678136 EUDAMED
EMDN Code
W01010232 URIC ACID EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

A-800 Ua by PZ CORMAY Spółka Akcyjna — 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
PL-MF-000023053

Sources (1)

  • EUDAMED cc4d0ea6-6bcb-4c50-b89d-ae3cc4278923 61 fields · synced Jul 13, 2026