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Lamitrode Tripole™

by Abbott Medical EUDAMED

Active European Union

Ref 3219

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5415067SCS0001L4 Basic UDI-DIDate29 Jun 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  • Withdrawn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 750959 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    24 Jun 2026
    Expires
    11 Oct 2027
    Reason
    Add device or group

Specification

EUDAMED

Device Name
Spinal Cord Stimulation
Model / Reference
3219
Primary DI / UDI-DI
05415067047908
Basic UDI-DI
5415067SCS0001L4
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

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