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  • 2017-12-28

    Happy New Year
            Happy New Year 
  • 2017-10-31

    ESH International Protocol Revision 2010
    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 pr...
  • 2017-10-24

    2017 MEDICA Invitation Booth# Hall16C30 Nov13-16
     2017 MEDICA Invitation Exhibitiona Name: The 2017 MEDICA Exhibition Location: Dusseldorf Germany Exhibition Date:November 13-16, 2017  Our Booth: Hall 16C30  We sincerely invite you and your comp...
  • 2017-09-13

    Sejoy-Board of Directors of CCCMHPE
    Congratulations! Sejoy are the Director, 7th Session of Board of Directors, CCCMHPE
  • 2017-08-04

    FIME 2017
    Please welcome to visit us at Booth#A.P74 FIME SHOW 2017   AUGUST 8-10, 2017 | 10:00 AM - 05:00 PM ORANGE COUNTY CONVENTION CENTER - WEST CONCOURSE, ORLANDO, FLORIDA      
  • 2016-10-05

    Understanding the FDA’s Unique Device Identification (UDI) System: Key Requirements and Implementation
    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 fi...
  • 2016-01-05

    Sejoy successfully finished FDA Audit
    Sejoy successfully finished FDA field Audit!!
  • 2015-12-28

    Unique Device Identification – UDI
    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...
  • Total 38 pages  Go to Page
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