bioMérieux SA

6 devices in the database

  • Model / Serial
    520518 ETEST®OXACILLIN OX 256 WW F100 520518 1003055340 01-Apr-2017 1003315740 28-Jul-2017 1004070580 08-Jun-2018 1004319590 22-Sep-2018 1004818850 21-Apr-2019 1004890270 24-May-2019 1005366110 12-Dec-2019 520558 ETEST®OXACILLIN OX 256 US F100 1003059010 01-Apr-2017 1003315830 28-Jul-2017 1004071250 08-Jun-2018 1004818860 21-Apr-2019 1004890400 24-May-2019
  • Model / Serial
  • Model / Serial
    1003987950 11/02/2016 1004061730 01/03/2016 1004084290 26/03/2016 1004105910 02/04/2016 1004119920 11/04/2016 1004163410 26/04/2016 1004194060 03/05/2016 1004210630 16/05/2016 1004255080 20/05/2016 1004261950 31/05/2016 1004296300 28/06/2016 1004307590 03/07/2016 1004355660 18/07/2016 1004392080 29/07/2016 1004430660 16/08/2016 1004439320 22/08/2016 1004487160 12/09/2016 1004504650 18/09/2016 1004520730 27/09/2016 1004533690 29/09/2016 1004614010 14/11/2016
  • Model / Serial
One more

19 manufacturers with a similar name

Learn more about the data here

  • Source
    LAANSM
  • 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
14 more