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Gynix

by Schultz Medical (UK) Ltd United Kingdom EUDAMED

Ref SM-BF/KS x10

EMDN U0903010101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-15060697809968 Basic UDI-DIDate19 Feb 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
SM-BF/KS x10: Sterile, Single Use, Gynix® Biopsy & Grasping Forceps, 5F / 1.67mm, 40cm
Model / Reference
SM-BF/KS x10
Primary DI / UDI-DI
15060697809968
Basic UDI-DI
B-15060697809968
EMDN Code
U0903010101 Cold biopsy forceps for urogenital endoscopy, single-use
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
UK-MF-000038582
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Schultz Medical (UK) Ltd

See all devices from Schultz Medical (UK) Ltd →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 9d1606e2-1d75-4f4e-b80d-07f7d95423a1 61 fields · synced 23 Oct 2026