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BRCAaccuTest™ PLUS

by NGeneBio Co., Ltd. EUDAMED

Active European Union

Ref NGB112V

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number880953987NGB112VVT Basic UDI-DIDate24 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
BRCAaccuTest PLUS
Model / Reference
NGB112V
Primary DI / UDI-DI
08809539870014
Basic UDI-DI
880953987NGB112VVT
EMDN Code
W01060203 Brca 1+2
Device Class
Class C
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
KR-MF-000042887
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from NGeneBio Co., Ltd.

See all devices from NGeneBio Co., Ltd. →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No