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Soflex Med D 30/10

by Στρωματοποιια Αθηνων Επε Greece EUDAMED

Ref SOFLEX MED D 30/10Model SOFLEX MED D EMDN V08068002

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5207003MTSOFLEXMEDASR Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Soflex Med D
Model / Reference
SOFLEX MED D, SOFLEX MED D 30/10
Primary DI / UDI-DI
52070030108376
Basic UDI-DI
5207003MTSOFLEXMEDASR
EMDN Code
V08068002 Bed supports
Device Class
Class I
Market of Registration
Cyprus

Manufacturer details

EUDAMED SRN
EL-MF-000043080

Other devices from Στρωματοποιια Αθηνων Επε

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 46d8c549-d068-4f12-8e25-5f8c2d33d05e 61 fields · synced 24 Oct 2026