bioMérieux SA

34 dispositifs dans la base de données

  • Modèle / numéro de série
    Catalog Number: 415603, 411402
  • Description du dispositif
    Diagnostic medical devices in vitro
  • Modèle / numéro de série
    Catalog Number: 505518, 505558 Batch Number: 505518 - lots 1002774320, 1002377890, 1002590470 505558 - lots 1002775330, 1002379610
  • Description du dispositif
    Diagnostic medical devices in vitro
  • Modèle / numéro de série
    Serial Number: Ref. 43371 - Lot 1004119200 Ref. 43371 - Lot 1004044190 Ref. 43371 - Lot 1004085400 Ref. 43466 - Lot 1004158090 Ref. 43466 - Lot 1004091980 Ref. 43466 - Lot 1004113000 Ref. 43466 - Lot 1004141170 Ref. 414524 – Lot 1004141270 Ref. 414524 – Lot 1004105600 Ref. 43466 - Lot 1004113000 Ref. 43466 - Lot 1004141170 Ref. 414524 – Lot 1004141270 Ref. 414524 – Lot 1004105600
  • Description du dispositif
    Diagnostic medical devices in vitro
  • Modèle / numéro de série
    Catalog Number: 414518 415358 416192 416546 417191 419071 419072 Model Number: All installed systems connected to a VITEK2 system Serial Number: 414518 2013 415358 2013 - 2015 416192 2013 - 2015 416546 2014 - 2015 417191 2015 - on going 419071 2015 - on going 419072 2015 - on going
  • Description du dispositif
    Diagnostic medical devices in vitro
  • Modèle / numéro de série
    Catalog Number: 412433 - 412434 - 521418 - 421458
  • Description du dispositif
    Diagnostic medical devices in vitro
29 en plus

19 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Source
    LAANSM
  • 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
14 en plus