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Disposable Biopsy Forceps

by Zhejiang Soudon Medical Technology Co., Ltd EUDAMED

Active European Union

Ref SD-01-F2320J-YModel SD-01-A、SD-01-B、SD-01-C、SD-01-D、SD-01-E、SD-01-F、SD-01-G、SD-01-H

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697513704BF01F6 Basic UDI-DIDate13 May 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR 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

Model / Reference
SD-01-A、SD-01-B、SD-01-C、SD-01-D、SD-01-E、SD-01-F、SD-01-G、SD-01-H, SD-01-F2320J-Y
Primary DI / UDI-DI
06975137041414
Basic UDI-DI
697513704BF01F6
EMDN Code
G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
Device Class
Class IIa
Market of Registration
Malta

Manufacturer details

EUDAMED SRN
CN-MF-000021047
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Zhejiang Soudon Medical Technology Co., Ltd

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Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: 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