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ANGUIS Guidewire

by Sungjin-Hitech Co., Ltd EUDAMED

Active European Union

Ref GW-15J21150

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800023714531 Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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

Model / Reference
GW-15J21150
Primary DI / UDI-DI
08800023714531
Basic UDI-DI
B-08800023714531
EMDN Code
C04030101 Diagnostic coronary and peripheral vascular guide wires, hydrophilic
Device Class
Class IIa
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
KR-MF-000036002
Authorised representative
Meridius Medical Europe Limited IE-AR-000004258

Other devices from Sungjin-Hitech Co., Ltd

See all devices from Sungjin-Hitech Co., Ltd →

Properties

  • Sterile

Other properties (12)

  • 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