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Cable Set

by Cerus Endovascular, Ltd. EUDAMED

Withdrawn Not intended for the EU market

Ref CAB701-01Model 0858644007CAB86

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0858644007CAB86 Basic UDI-DIDate16 Jul 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000307203 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    13 Apr 2026
    Expires
    20 Jun 2029
    Reason
    Change approved

Specification

EUDAMED

Device Name
Cable Set CAB701-01
Model / Reference
0858644007CAB86, CAB701-01
Primary DI / UDI-DI
00858644007943
Basic UDI-DI
0858644007CAB86
EMDN Code
C010402020399 Embolisation devices - other
Device Class
Class I

Manufacturer details

EUDAMED SRN
GB-MF-000008548
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Cerus Endovascular, Ltd.

See all devices from Cerus Endovascular, 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