Skip to content

Teeter

by STL International, Inc.; DBA-Teeter United States EUDAMED

Ref Dex II

EMDN Z12130201

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0759265DEXIIXA Basic UDI-DIDate17 Mar 2026RegisteredStatusActive

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
Dex II Commercial Inversion & Core Training System
Model / Reference
Dex II
Primary DI / UDI-DI
00759265000019
Basic UDI-DI
0759265DEXIIXA
Direct Marketing DI
00759265000019
EMDN Code
Z12130201 Traction beds
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000024237
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from STL International, Inc.; DBA-Teeter

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 fc48f18a-8c4f-4574-b9ae-33ef0f6baa07 61 fields · synced 22 Oct 2026