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SensiScreen

EUDAMED

Class IVD General (EU MDR)

Ref 5525; 5530; 5535; 5336; 5341; 5346Model BRAF qPCR Assay

by PentaBase A/S

Identity

Trade Name
SensiScreen EUDAMED
Device Name
SensiScreen® Liquid BRAF qPCR Assay EUDAMED
Model / Reference
BRAF qPCR Assay EUDAMED
5525; 5530; 5535; 5336; 5341; 5346 EUDAMED

Identifiers

Primary DI / UDI-DI
D-5713915SS002V5Q8 EUDAMED
Basic UDI-DI
B-5713915SS002V5Q8 EUDAMED
EMDN Code
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Denmark 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

SensiScreen by PentaBase A/S — 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
PentaBase A/S
EUDAMED SRN
DK-MF-000023157

Sources (2)

  • EUDAMED 0717248c-3d46-4640-99d6-9af1ba0584be 61 fields · synced Jun 20, 2026
  • EUDAMED 0717248c-3d46-4640-99d6-9af1ba0584be-1 61 fields · synced Jun 10, 2026