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Disposable Biopsy Forceps

by Zhejiang Soudon Medical Technology Co., Ltd 306 variants

Ref SD-01-A2318J-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

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697513704BF01F6 Basic UDI-DI 06975137040530UDI-DIDate13 May 2025RegisteredStatusActive

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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

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-A2318J-Y
Primary DI / UDI-DI
06975137040530
Basic UDI-DI
697513704BF01F6
EMDN Code
G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
Device Class
Class IIa
EU market of registration
Malta

Manufacturer details

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

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Properties

Other properties (13)

  • Sterile: No
  • 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