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Cardiohealth

by Cardiohealth Tibbi Urunler A.S. 153 variants

Ref GC7JL50

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868415961GC7JL50N2 Basic UDI-DI 86841596117006UDI-DIDate1 Jul 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Guiding Catheter Procedure Pack
Model / Reference
GC7JL50
Primary DI / UDI-DI
86841596117006
Basic UDI-DI
868415961GC7JL50N2
EMDN Code
C0104020204, C058001
Device Class
Class IIa
Medical Purpose
Perifer Kılavuz Kateter; periferal vasküler girişimler sırasında balon kateterler, kılavuz teller ve diğer girişimsel tıbbi cihazların damar lümenine güvenli ve kontrollü şekilde iletilmesini sağlamak amacıyla kullanılan tıbbi bir cihazdır. Bu ürün yalnızca periferal vasküler uygulamalar için tasarlanmıştır.

Manufacturer details

EUDAMED SRN
TR-PR-000036994

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Properties

  • Sterile