Randox Liquid Cardiac Control


  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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.
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  • Modelo / Serial
  • Manufacturer
  • Modelo / Serial
    Randox Liquid Cardiac Controls when used with CKMB and Myoglobin assays. An in vitro diagnostic medical device (IVD)Liquid Cardiac Control 1Catalogue Number: CQ5051Batch Numbers: 3909CK, 3913CK (exp. 28 Oct 2017), 3987CK (exp. 28 Apr 2018)Liquid Cardiac Control 2Catalogue Number: CQ5052Batch Numbers: 3911CK (exp. 28 Oct 2017), 3991CK (exp. 28 Apr 2018)Liquid Cardiac Control 3Catalogue Number: CQ5053Batch Numbers: 3912CK (exp. 28 Oct 2017)ARTG Number: 208141
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