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Proteus OX19

EUDAMED

Class IVD General (EU MDR)

Ref 5111

by Cypress Diagnostics

Identity

Trade Name
Proteus OX19 EUDAMED
Device Name
Proteus OX19 EUDAMED
Model / Reference
5111 EUDAMED

Identifiers

Primary DI / UDI-DI
05404035102084 EUDAMED
Basic UDI-DI
B-05404035102084 EUDAMED
EMDN Code
W0105011705 RICKETTSIA EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Belgium 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

Proteus OX19 by Cypress Diagnostics — 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

Manufacturer
Cypress Diagnostics
EUDAMED SRN
BE-MF-000000033

Sources (1)

  • EUDAMED 31342b93-ccf9-4af2-8fe2-b39807535194 61 fields · synced Jun 18, 2026