Becton, Dickinson & Company

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Description

19 dispositivos en la base de datos

  • Modelo / Serial
    659293 | 7038969, 7243868, 7248685, 7317597
  • Descripción del producto
    IVD: Multiple mature lymphocyte cell marker IVD, kit, fluorescent activated cell sorting/flow cytometry (FACS/Flow)
  • Modelo / Serial
    448103, 448620, 448746, 448764, 448781, 448790, 448792, 448794, 448874, 448875, 448877, 448878, 449001, 449025, 449026 | All
  • Descripción del producto
    IVD: Bacteriology - Identification & Susceptibility Testing
  • Modelo / Serial
    342417 | 13532,18636,29783,33552,40550,70946,09831,20936,25555,31761,
    31864,51629,51897,84976,94769
  • Descripción del producto
    IVD: Cell surface receptor recognizing antibody kit
  • Modelo / Serial
    342447 | see FSN
  • Descripción del producto
    IVD: Cell surface receptor recognizing antibody kit
  • Modelo / Serial
    335833 | 5218762; 5348579
  • Descripción del producto
    IVD: B/T-cell subtyping antibody kit
14 más

22 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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
17 más