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Standard

by Fysiotech OÜ Estonia EUDAMED

Ref 10203Model X1

EMDN V080603

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number47450102451020392 Basic UDI-DIDate28 Feb 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Standard
Model / Reference
X1, 10203
Primary DI / UDI-DI
04745010245107
Basic UDI-DI
47450102451020392
Direct Marketing DI
04745010245107
EMDN Code
V080603 Treatment, diagnosis and monitoring medical beds
Device Class
Class I
Market of Registration
Estonia

Manufacturer details

EUDAMED SRN
EE-MF-000007651

Other devices from Fysiotech OÜ

See all devices from Fysiotech OÜ →

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 78822c92-e241-4dc5-8e37-c19c8831275e 61 fields · synced 22 Oct 2026