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Uriflet S 9UB

EUDAMED

Class IVD General (EU MDR)

Ref 23905

by ARKRAY Factory, Inc.

Identity

Trade Name
Uriflet S 9UB EUDAMED
Device Name
Uriflet S 9UB EUDAMED
Model / Reference
23905 EUDAMED

Identifiers

Primary DI / UDI-DI
D-23905GG EUDAMED
Basic UDI-DI
B-23905GG EUDAMED
EMDN Code
W0101060205 URINE MULTI-CONSTITUENT TEST STRIPS (AUTOMATED) EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy 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

Uriflet S 9UB by ARKRAY Factory, Inc. — 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
JP-MF-000003008
Authorised Representative
ARKRAY Europe, B.V. NL-AR-000002056

Sources (1)

  • EUDAMED 78b34b38-7c6c-4d90-85e0-3d913f76a3c6 61 fields · synced Jun 18, 2026