Skip to content

ICL Forceps Ribbed

by Sihong Ophsurin Co., Ltd. EUDAMED

Active European Union

Ref RU-S143-T13H0N 25G（TV-11578-3）

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697504445RFORCEPSJP Basic UDI-DIDate12 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • 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

Device Name
Reusable Ophthalmic Forceps
Model / Reference
RU-S143-T13H0N 25G（TV-11578-3）
Primary DI / UDI-DI
06975044457636
Basic UDI-DI
697504445RFORCEPSJP
EMDN Code
L170201 Ophthalmic grasping forceps, reusable
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000037458
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Sihong Ophsurin Co., Ltd

See all devices from Sihong Ophsurin Co., Ltd →

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