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Medibord Mirak S1

by Medibord Limited EUDAMED

Withdrawn No longer placed on the EU market

Ref SSMR-RT

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5065006061MedibordX9 Basic UDI-DIDate25 Mar 2024RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Patient Support Boards, Coil Holders and Indexing Bars. Variations and sizes described in the technical documentation.
Model / Reference
SSMR-RT
Primary DI / UDI-DI
05065006061009
Basic UDI-DI
5065006061MedibordX9
Direct Marketing DI
05065006061009
EMDN Code
V0804 PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures)
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
UK-MF-000038315
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Medibord Limited

See all devices from Medibord Limited →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • 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