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Rumel Thoracic Forceps

by Acheron Instruments (Private) Limited EUDAMED

Active European Union

Ref AI-GS-02-426

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++G733RUMELTHORAC0169 Basic UDI-DIDate11 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Rumel Thoracic Forceps
Model / Reference
AI-GS-02-426
Primary DI / UDI-DI
+G733AIGS024260R
Basic UDI-DI
++G733RUMELTHORAC0169
EMDN Code
L07080102 Generic vascular clamping angiostats and forceps, reusable
Device Class
Class I
Market of Registration
Hungary

Manufacturer details

EUDAMED SRN
PK-MF-000037497
Authorised representative
KHANG BAO INTERNATIONAL KFT HU-AR-000034102

Other devices from Acheron Instruments (Private) Limited

See all devices from Acheron Instruments (Private) Limited →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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