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Extractor™ Aspiration Catheter

by GENOSS Co., Ltd. 2 variants

Ref GAC-6-110

Active European Union

CE MDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08809324764047 Basic UDI-DI 08809324764047UDI-DIDate17 Sep 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Aspiration Thrombectomy Catheter
Model / Reference
GAC-6-110
Primary DI / UDI-DI
08809324764047
Basic UDI-DI
B-08809324764047
EMDN Code
C010401020501 Manual cardiac thrombectomy and thromboaspiration systems
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
KR-MF-000029064
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Genoss

See all devices from Genoss →

Properties

  • 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