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Wright

EUDAMED

Class A (EU MDR)

Ref HS023

by Cypress Diagnostics

Identity

Trade Name
Wright EUDAMED
Device Name
Wright EUDAMED
Model / Reference
HS023 EUDAMED

Identifiers

Primary DI / UDI-DI
05404035100226 EUDAMED
Basic UDI-DI
54040351HS0236B EUDAMED
Direct Marketing DI
05404035100226 EUDAMED
EMDN Code
W0103010302 ROMANOWSKY STAINS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Belgium 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

New Device

No

EUDAMED

Wright by Cypress Diagnostics — 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

Manufacturer
Cypress Diagnostics
EUDAMED SRN
BE-MF-000000033

Sources (1)

  • EUDAMED f12bcf3c-a745-46a6-89b1-62870edec516 61 fields · synced Jul 9, 2026