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Sensititre Euenc2f

EUDAMED

Class B (EU MDR)

Ref EUENC2F

by Trek Diagnostic Systems Ltd

Identity

Trade Name
SENSITITRE EUENC2F EUDAMED
Device Name
SENSITITRE EUENC2F EUDAMED
Model / Reference
EUENC2F EUDAMED

Identifiers

Primary DI / UDI-DI
05032384584468 EUDAMED
Basic UDI-DI
5032384EUENC2FNE EUDAMED
EMDN Code
W0104080108 GRAM POSITIVE SUSCEPTIBILITY TESTING - AUTOMATED 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 Euenc2f 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 fe87d2f9-4897-467c-b668-a1890a80460c 61 fields · synced Jun 19, 2026