Skip to content

Gynix

by Schultz Medical (UK) Ltd United Kingdom EUDAMED

Ref SM-BF/KS

EMDN U0903010101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060697809961 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 22 Oct 2026

Device Name
SM-BF/KS: Sterile, Single Use, Gynix® Biopsy & Grasping Forceps, 5F / 1.67mm, 40cm
Model / Reference
SM-BF/KS
Primary DI / UDI-DI
05060697809961
Basic UDI-DI
B-05060697809961
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 c1ec75e0-2995-49c5-942c-9a9894dc6023 61 fields · synced 22 Oct 2026