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SAI Delivery Catheter

by HighLife France EUDAMED

Ref 631102-2

EMDN P07038002

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number2292597CE01 Date31 Jul 2026IssuedStatusActive expires 1 Jan 2031

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 2292597CE01 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0344
    Issued
    31 Jul 2026
    Expires
    1 Jan 2031
    Reason
    Add device or group
  • 2292597TD01 Amended

    Technical documentation EU MDR

    Notified body
    Notified body 0344
    Issued
    31 Jul 2026
    Expires
    1 Jan 2031
    Reason
    Other

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
631102-2
Primary DI / UDI-DI
00850035587027
Basic UDI-DI
0850035587631102-266
EMDN Code
P07038002 Cardiac valve transcatheter implant accessories
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
FR-MF-000015887

Other devices from HighLife

See all devices from HighLife →

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 817e7030-2c91-4d33-8576-f3519f6e8abd 61 fields · synced 24 Oct 2026