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Navigo 4LV Arc 88

by MicroPort CRM S.r.l. Italy EUDAMED

Ref TLT022CModel NAVIGO 4LV

EMDN J0190010103

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberG70 005178 0044 Date14 Sep 2026IssuedStatusActive expires 12 Dec 2031

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

    Issued
    14 Sep 2026
    Expires
    12 Dec 2031
    Valid from
    13 Dec 2026

Specification

EUDAMED · synced 24 Oct 2026

Device Name
NAVIGO 4LV Lead
Model / Reference
NAVIGO 4LV, TLT022C
Primary DI / UDI-DI
08031527019710
Basic UDI-DI
8031527NAVIGO0000000001EF
EMDN Code
J0190010103 Left ventricular leads with coronary sinus cannulation system (triple chamber p.m.)
Device Class
Class III
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029013

Other devices from MicroPort CRM S.r.l.

See all devices from MicroPort CRM S.r.l. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
  • Incorporates Medicinal Product
Other properties (10)
  • 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

Sources (1)

  • EUDAMED 9e506a9d-1ac6-443b-bf3f-4201b206efea 61 fields · synced 24 Oct 2026