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Quik-Check Expert U500 Urine Analyzer

EUDAMED

Class A (EU MDR)

Ref U213-117-201

by Acon Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
Quik-Check Expert U500 Urine Analyzer EUDAMED
Device Name
Expert U500 Urine Analyzer EUDAMED
Model / Reference
U213-117-201 EUDAMED

Identifiers

Primary DI / UDI-DI
26921756496405 EUDAMED
Basic UDI-DI
6921756499990026X7 EUDAMED
EMDN Code
W020101020102 SEMI-AUTOMATED URINE ANALYSERS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Quik-Check Expert U500 Urine Analyzer by Acon Biotech (Hangzhou) Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000006977
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED d5a1512c-5a63-4707-957e-9abb455d72fa 61 fields · synced Jun 18, 2026