CoaguChek

Fabricant

  • 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

75 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    11911822; 20646321; 20335921 || 23343322; 23194921; 23073621.
  • Description du dispositif
    REAGENTS, CONTROLS AND CALIBRATORS USED IN DETERMINATIONS OF THE COAGULATION AREA APPARATUS OF SAMPLES OF HUMAN ORIGIN.
  • Manufacturer
  • Modèle / numéro de série
    Model: Models: 04625412019, 04800842190, 05530199190, 04625374190, 04625358019, 04625315019, Affected: All serial numbers
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    In-vitro diagnostics
  • Manufacturer
  • Modèle / numéro de série
    All units.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    United States
  • Description du dispositif
    CoaguChek Pro DM meter; catalog # 1894048 and 1893211.
  • Manufacturer
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