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ΟΥΡΙΚΟ ΟΞΥ LIQUID R1:8x40 R2:4x20 ml (HIT)

EUDAMED

Class IVD General (EU MDR)

Ref 001741

by Biotechnological Applications Ltd

Identity

Trade Name
ΟΥΡΙΚΟ ΟΞΥ LIQUID R1:8x40 R2:4x20 ml (HIT) EUDAMED
Device Name
ΟΥΡΙΚΟ ΟΞΥ LIQUID R1:8x40 R2:4x20 ml (HIT) EUDAMED
Model / Reference
001741 EUDAMED

Identifiers

Primary DI / UDI-DI
05213003192930 EUDAMED
Basic UDI-DI
B-05213003192930 EUDAMED
EMDN Code
W01010232 URIC ACID EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Greece 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

ΟΥΡΙΚΟ ΟΞΥ LIQUID R1:8x40 R2:4x20 ml (HIT) by Biotechnological Applications 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
GR-MF-000033000

Sources (1)

  • EUDAMED 50f5d508-9f9e-489e-9233-136bb8ba28e1 61 fields · synced Jul 24, 2026