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SlimTip™

by Abbott Medical EUDAMED

Active European Union

Ref MN20450-50A

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5415067DRG0001E4 Basic UDI-DIDate13 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 725783 Reissued

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    30 Jun 2026
    Expires
    4 Jul 2031
    Valid from
    4 Jul 2026

Specification

EUDAMED

Device Name
Dorsal Root Ganglion Stimulation
Model / Reference
MN20450-50A
Primary DI / UDI-DI
05415067027368
Basic UDI-DI
5415067DRG0001E4
EMDN Code
J020203 Spinal neurostimulation leads
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000028918
Authorised representative
Abbott Medical BE-AR-000008744

Other devices from Abbott Medical

See all devices from Abbott Medical →

Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No