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DERIVO 2 Embolisation Device

by Acandis GmbH Germany EUDAMED

Ref 01-107027

EMDN P0799

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426065033DERIVO2AC Basic UDI-DIDate17 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 1000302303 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 0297
    Issued
    16 Mar 2026
    Expires
    17 Jul 2029
    Reason
    Change approved
  • 1000331236 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    6 Aug 2026
    Expires
    22 Mar 2028
    Reason
    Change approved

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
01-107027
Primary DI / UDI-DI
04260650339240
Basic UDI-DI
426065033DERIVO2AC
Direct Marketing DI
04260650339240
EMDN Code
P0799 Vascular and cardiac prostheses - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006259

Other devices from Acandis GmbH

See all devices from Acandis GmbH →

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 04260650339240|426065033DERIVO2AC 61 fields · synced 24 Oct 2026