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Cardiohealth

by Cardiohealth Tibbi Urunler A.S. 153 variants

Ref AC4AL3

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868415961AC4AL3DD Basic UDI-DI 86841596135376UDI-DIDate2 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  • Withdrawn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
Angiography Catheter Procedure Pack
Model / Reference
AC4AL3
Primary DI / UDI-DI
86841596135376
Basic UDI-DI
868415961AC4AL3DD
EMDN Code
C0104010101, C058001
Device Class
Class IIa
Medical Purpose
Periferik Anjiyografi kateteri kontrast madde uygulaması, görüntüleme ve tanının dahil olduğu çeşitli tıbbi amaçlar için vasküler dolaşıma girişte kısa süreli kullanım için tasarlanmış bir medikal cihazdır.

Manufacturer details

EUDAMED SRN
TR-PR-000036994

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Properties

  • Sterile