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Thermablate EAS

by Idoman Teoranta Ireland EUDAMED

Ref 22001

EMDN Z12080201

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05392000074118 Basic UDI-DIDate19 Oct 2021RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Thermablate EAS Treatment Control Unit
Model / Reference
22001
Primary DI / UDI-DI
05392000074118
Basic UDI-DI
B-05392000074118
EMDN Code
Z12080201 Endometrial ablation equipment
Device Class
Class IIb
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000000090

Other devices from Idoman Teoranta

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED e88e3dfb-1cbc-4bc1-a3f1-528afdc59a0e 61 fields · synced 24 Oct 2026