Becton, Dickinson & Company

5 devices in the database

  • Model / Serial
    443376
  • Product Description
    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)
  • Model / Serial
    443710
  • Product Description
    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)
  • Model / Serial
  • Product Description
    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)
  • Model / Serial
  • Product Description
    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)
  • Model / Serial
    221606, 221607 | 4042455, 4067180, 4087204, 4127564
  • Product Description
    IVD: Culture medium, transport

22 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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 more