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Sensititre Begnuz

EUDAMED

Class B (EU MDR)

Ref BEGNUZ

by Trek Diagnostic Systems Ltd

Identity

Trade Name
SENSITITRE BEGNUZ EUDAMED
Device Name
SENSITITRE BEGNUZ EUDAMED
Model / Reference
BEGNUZ EUDAMED

Identifiers

Primary DI / UDI-DI
05032384549368 EUDAMED
Basic UDI-DI
5032384BEGNUZLB EUDAMED
EMDN Code
W0104080599 MANUAL SUSCEPTIBILITY TESTING - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Sensititre Begnuz by Trek Diagnostic Systems Ltd — Class B — 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
GB-MF-000016922
Authorised Representative
Thermo Fisher Diagnostics B.V. NL-AR-000013157

Sources (1)

  • EUDAMED 66a06aec-e6f6-4b28-9b49-23601d69b2da 61 fields · synced Jul 9, 2026