Becton, Dickinson & Company

5 dispositifs dans la base de données

  • Modèle / numéro de série
    443376
  • Description du dispositif
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • Modèle / numéro de série
    443710
  • Description du dispositif
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • Modèle / numéro de série
  • Description du dispositif
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • Modèle / numéro de série
  • Description du dispositif
    IVD: Endocervical/vaginal specimen collection kit, liquid transport medium; Multiple vaginitis-associated organism and Multiple sexually transmitted pathogen nucleic acid IVD, kit, nucleic acid technique (NAT)
  • Modèle / numéro de série
    221606, 221607 | 4042455, 4067180, 4087204, 4127564
  • Description du dispositif
    IVD: Culture medium, transport

22 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
  • 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
17 en plus