Luminex Corporation

  • Adresse du fabricant
    Luminex Corporation, 12212 Technology Blvd, Austin TX 78727-6101
  • Société-mère du fabricant (2017)
  • Source
    USFDA
  • 1 Event

Un dispositif médical dans la base de données

  • Modèle / numéro de série
    ARIES System UDI: 00840487101537 and ARIES M1 System UDI: 00840487100080
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US Distribution and to the countries of Finland and China.
  • Description du dispositif
    ARIES System and ARIES M1 System

4 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
  • Adresse du fabricant
    Luminex Corporation, 12212 Technology Blvd, Austin TX 78727-6131
  • Société-mère du fabricant (2017)
  • Source
    USFDA