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Treat

by Fysiotech OÜ Estonia EUDAMED

Ref 10802, 20846AModel 2, 846A

EMDN V080603

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4745010245108029W Basic UDI-DIDate6 Sep 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
2, 10802, 846A, 20846A
Primary DI / UDI-DI
04745010245060, 04745010245152
Basic UDI-DI
4745010245108029W, 474501024520846A69
Direct Marketing DI
04745010245060
04745010245152
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 (2)

  • EUDAMED ebfc8532-dead-4e95-8562-5f25be7bbed6 61 fields · synced 22 Oct 2026
  • EUDAMED 04745010245152|474501024520846A69 61 fields · synced 19 May 2026