Industry News

  • ESH International Protocol Revision 2010
    Post time: 10-31-2017

    The International Protocol for the validation of blood pressure measuring devices in adults was revised by the European Society of Hypertension in 20101. A number of modifications in the revised protocol acknowledge that device accuracy has improved with technological advancements, and the passin...Read more »

  • UDI Basics
    Post time: 10-05-2016

    In 2013, the Food and Drug Administration (FDA) released a final rule establishing a unique device identification system designed to adequately identify devices through distribution and use. The final rule requires device labelers to include a unique device identifier (UDI) on device labels and p...Read more »

  • Unique Device Identification – UDI
    Post time: 12-28-2015

    FDA is establishing a unique device identification system to adequately identify medical devices through their distribution and use. When fully implemented, the label of most devices will include a unique device identifier (UDI) in human- and machine-readable form. Device labelers must also submi...Read more »

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