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Rotab

by Genourob France EUDAMED

Ref ROTABModel LDA

EMDN V030202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number37012090LDAQ8 Basic UDI-DIDate15 Jan 2026RegisteredStatusActive
European UnionCE/MDR Number37012090LDAQ8 Basic UDI-DIDate15 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDD, CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
LDA, ROTAB
Primary DI / UDI-DI
03701209000057, D-ROTAB7F
Basic UDI-DI
37012090LDAQ8, B-ROTAB7F
EMDN Code
V030202 Goniometers
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000029224

Other devices from Genourob

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 9d7758aa-706f-4be6-85d8-1ed0e69f20ff 61 fields · synced 22 Oct 2026
  • EUDAMED D-ROTAB7F|B-ROTAB7F 61 fields · synced 8 Oct 2026