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Navigo 4LV 2D 78/Arc 78 Re-Intervention Kit 78

by MicroPort CRM S.r.l. Italy EUDAMED

Ref RLK05CModel NAVIGO RE-INTERVENTION KIT

EMDN J01900180

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8031527STYLETSKIT000001FR Basic UDI-DIDate25 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 005178 0044 Reissued

    Technical documentation EU MDR

    Notified body
    TÜV SÜD Product Service GmbH 0123
    Issued
    14 Sep 2026
    Expires
    12 Dec 2031
    Valid from
    13 Dec 2026

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Navigo Re-Intervention Kit
Model / Reference
NAVIGO RE-INTERVENTION KIT, RLK05C
Primary DI / UDI-DI
08031527019840
Basic UDI-DI
8031527STYLETSKIT000001FR
EMDN Code
J01900180 Permanent cardiac leads - accessories
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029013

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 80852c80-c2f3-43d3-8dee-4a86af440f1f 61 fields · synced 24 Oct 2026