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Non-Sterile Reusable Biopsy Forceps

by G-Flex Flexible Instruments Europe Belgium EUDAMED

Ref GF230S EMDN G030799

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number54200513-TF17-BBF-RU-6Q Basic UDI-DIDate8 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • BE25/00000030 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 1639
    Issued
    21 Aug 2026
    Expires
    29 Jan 2030
    Reason
    Add device or group

Specification

EUDAMED · synced 25 Oct 2026

Model / Reference
GF230S
Primary DI / UDI-DI
05420051301003
Basic UDI-DI
54200513-TF17-BBF-RU-6Q
EMDN Code
G030799 Gastrointestinal endoscopy, diagnostic devices - other
Device Class
Class I
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000000623

From the manufacturer

Manufacturer's product page: Disposable & Reusable Biopsy Forceps

Other devices from G-Flex Flexible Instruments Europe

See all devices from G-Flex Flexible Instruments Europe →

Properties & raw data

Show properties, registry sources and raw records
  • Reusable
  • Reprocessed
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 05420051301003|54200513-TF17-BBF-RU-6Q 61 fields · synced 25 Oct 2026