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Laport

by SEJONG MEDICAL Co., Ltd. South Korea EUDAMED

Ref LT22-0310

EMDN K01010101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08806182201066 Basic UDI-DIDate12 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
LT22-0310
Primary DI / UDI-DI
08806182201066
Basic UDI-DI
B-08806182201066
EMDN Code
K01010101 Trocar standard, single-use
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
KR-MF-000020090
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Sejong Medical Co., Ltd

See all devices from Sejong Medical Co., Ltd →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (10)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 3f72848b-1851-40d0-86dc-2c1c205c2bed 61 fields · synced 24 Oct 2026