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Neqstent

by Cerus Endovascular, Ltd. EUDAMED

Active European Union

Ref NQS414-15Model 0850014958CNSPFVZ

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0850014958CNSPFVZ Basic UDI-DIDate17 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 1000307201 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 0297
    Issued
    13 Apr 2026
    Expires
    20 Jun 2029
    Reason
    Change approved
  • 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
Contour Neurovascular System Product Family (CNSPF)
Model / Reference
0850014958CNSPFVZ, NQS414-15
Primary DI / UDI-DI
00850014958251
Basic UDI-DI
0850014958CNSPFVZ
EMDN Code
C010404020299 Neurovascular embolisation devices - other
Device Class
Class III
Market of Registration
Netherlands

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
  • Implantable

Other properties (11)

  • 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