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PRAEVAorta®

by Nurea France EUDAMED

Ref V.1.7.0Model Software

EMDN C0199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FRMF000000162KC Basic UDI-DIDate8 Feb 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
Software, V.1.7.0
Primary DI / UDI-DI
D-FRMF000000162KC
Basic UDI-DI
B-FRMF000000162KC
EMDN Code
C0199 Arterio-venous devices - other
Device Class
Class I
Special Device Type
-1192
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000162

Other devices from Nurea

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED aad5d5a7-1334-46bc-800f-2c2b33781486 61 fields · synced 22 Oct 2026