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aixstent OES

by bess pro gmbh EUDAMED

Active European Union

Ref 102-24-140

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4063106ASTAIXMP Basic UDI-DIDate10 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 1000310118 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0297
    Issued
    2 Jul 2026
    Expires
    1 Jul 2031
  • 1000301888 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    2 Jul 2026
    Expires
    27 Feb 2030
    Reason
    Change approved

Specification

EUDAMED

Device Name
aixstent
Model / Reference
102-24-140
Primary DI / UDI-DI
14063106100275
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006209

Other devices from bess pro gmbh

See all devices from bess pro gmbh →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (12)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: 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 27c1fd25-934f-47c1-a2cd-d96ba9fbd4a1 61 fields · synced 24 Oct 2026