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Cardiohealth

by Cardiohealth Tibbi Urunler A.S. 153 variants

Ref GC6JL40

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 Number86841596GC6JL40R7 Basic UDI-DI 86841596112810UDI-DIDate29 Jun 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  • Withdrawn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
GC6JL40
Primary DI / UDI-DI
86841596112810
Basic UDI-DI
86841596GC6JL40R7
EMDN Code
C0104020204, C058001
Device Class
Class IIa
Medical Purpose
kapalı periferik vaskuler cerrahi operasyonlar(Anjiyo operasyonları)

Manufacturer details

EUDAMED SRN
TR-PR-000036994

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Properties

  • Sterile