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Kleinert-Kutz's tendon seizing forceps, 200 mm

by SUBAN Kéziműszer Hungary Zártkörűen Működő Részvénytársaság EUDAMED

Active European Union

Ref RL-712-20

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5996660CsontfogokL9 Basic UDI-DIDate26 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Bone forceps
Model / Reference
RL-712-20
Primary DI / UDI-DI
05996660055144
Basic UDI-DI
5996660CsontfogokL9
Direct Marketing DI
05996660055144
EMDN Code
L07080104 Vascular approximators, reusable
Device Class
Class I
Market of Registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000006381

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Properties

  • 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