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Minotor 3 XL

by Benoit Systemes France EUDAMED

Ref 81MXLS30, 81MXCF30

EMDN Y122410

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number376034429MINOTOR/LDHM Basic UDI-DIDate17 Jun 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Trade Name
Minotor 3 XL
Minotor 3 XL Châssis fixe
Device Name
Minotor / Light Drive
Model / Reference
81MXLS30, 81MXCF30
Primary DI / UDI-DI
03760344291355, 03760344291430
Basic UDI-DI
376034429MINOTOR/LDHM
Direct Marketing DI
03760344291355
03760344291430
EMDN Code
Y122410 Electric propulsion unit
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000004445

Other devices from Benoit Systemes

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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 e809cbfa-0216-4ccf-a8db-c996d1e4aad5 61 fields · synced 22 Oct 2026
  • EUDAMED 03760344291430|376034429MINOTOR/LDHM 61 fields · synced 18 May 2026