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NEURESCUE Device

by Neurescue Aps 2 variants

Ref 400999-00Model 40000X

Active European Union

CE MDR

Valid until

11 Aug 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier TÜV SÜD Danmark

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 Number574400588000040000XAW Basic UDI-DI 25744005889992UDI-DIDate5 Feb 2026RegisteredStatusActive EUDAMED: not on the EU market

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • G11DK 133591 0001 Active

    Quality management system EU MDR

    Certifier
    TÜV SÜD Danmark 2443
    Issued
    12 Aug 2025
    Expires
    11 Aug 2030
  • G70DK 133591 0002 Active

    Technical documentation EU MDR

    Certifier
    TÜV SÜD Danmark 2443
    Issued
    12 Aug 2025
    Expires
    11 Aug 2030

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
40000X, 400999-00
Primary DI / UDI-DI
25744005889992
Basic UDI-DI
574400588000040000XAW
EMDN Code
C0104020103 Vascular occlusion catheters
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DK-MF-000010162

Other devices from Neurescue Aps

Properties

  • Sterile
  • Measuring Function

Other properties (11)

  • 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
  • Incorporates Medicinal Product: No