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Wiper kit

EUDAMED

Class A (EU MDR)

Ref ME-2323D

by Diamond Diagnostics Inc

Identity

Trade Name
Wiper kit EUDAMED
Device Name
Probe Wiper Kit EUDAMED
Model / Reference
ME-2323D EUDAMED

Identifiers

Primary DI / UDI-DI
00811403015962 EUDAMED
Basic UDI-DI
081140301ME2323DDT EUDAMED
EMDN Code
W05020199 SAMPLES TRANSPORT, CONTAINERS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Hungary 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

No

EUDAMED

New Device

No

EUDAMED

Wiper kit by DIAMOND DIAGNOSTICS Inc — 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
US-MF-000035435
Authorised Representative
Diamond Diagnostics Inc. Magyarországi Fióktelepe HU-AR-000034351

Sources (1)

  • EUDAMED bef8e94f-27f6-41e7-967f-ffb723f7ba92 61 fields · synced Jun 19, 2026