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Triever20

by Inari Medical, Inc. United States EUDAMED

Ref 21-101

EMDN C019002

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1000332280 Date25 Sep 2026IssuedStatusActive expires 8 Nov 2028

Coverage

1 jurisdiction

NorwaySwedenFinlandFinlandNorwaySwedenFinlandFinlandNorwaySwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceLiechtensteinAustriaHungaryFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

EU market availability

Available in 29 countries, as listed in EUDAMED:

  • Austriasince 14 Oct 2024
  • Belgiumsince 14 Oct 2024
  • Bulgariasince 14 Oct 2024
  • Croatiasince 14 Oct 2024
  • Cyprussince 14 Oct 2024
  • Czechiasince 14 Oct 2024
  • Denmarksince 14 Oct 2024
  • Estoniasince 14 Oct 2024
  • Finlandsince 14 Oct 2024
  • Francesince 14 Oct 2024
  • Germanysince 14 Oct 2024
  • Greecesince 14 Oct 2024
  • Hungarysince 14 Oct 2024
  • Irelandsince 14 Oct 2024
  • Italysince 14 Oct 2024
  • Latviasince 14 Oct 2024
  • Liechtensteinsince 14 Oct 2024
  • Lithuaniasince 14 Oct 2024
  • Luxembourgsince 14 Oct 2024
  • Maltasince 14 Oct 2024
  • Netherlandssince 14 Oct 2024
  • Northern Irelandsince 14 Oct 2024
  • Norwaysince 14 Oct 2024
  • Polandsince 14 Oct 2024
  • Portugalsince 14 Oct 2024
  • Slovakiasince 14 Oct 2024
  • Sloveniasince 14 Oct 2024
  • Spainsince 14 Oct 2024
  • Swedensince 14 Oct 2024

Last checked 24 Oct 2026.

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 1000336504 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 0297
    Issued
    25 Sep 2026
    Expires
    13 Oct 2029
    Reason
    Change approved
  • 1000332280 Restricted

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    25 Sep 2026
    Expires
    8 Nov 2028
    Reason
    Other

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
21-101
Primary DI / UDI-DI
00810123710034
Basic UDI-DI
081012371TRIEVCATH7G
Direct Marketing DI
00810123710034
EMDN Code
C019002 Embolectomy catheters
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000008693
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Inari Medical, Inc.

See all devices from Inari Medical, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED ec350ada-03da-48cb-85b1-953541ea26a3 61 fields · synced 24 Oct 2026