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ScolioSense

by Aidplex Μονοπροσωπη Ιδιωτικη Κεφαλαιουχικη Εταιρια EL EUDAMED

Ref SCLSNS1

EMDN Z12139099

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number521400263424082022PH Basic UDI-DIDate29 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Aidplex Scoliosis
Model / Reference
SCLSNS1
Primary DI / UDI-DI
05214002634018
Basic UDI-DI
521400263424082022PH
Direct Marketing DI
05214002634018
EMDN Code
Z12139099 Various orthopaedic and traumatology instruments - other
Device Class
Class I
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000040369

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 05214002634018|521400263424082022PH 61 fields · synced 23 Oct 2026