BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Spine Wave Navigated Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780362326·Integra® Miltex® McGuire Corneal Scissors 4-1/8...

    TOTAL SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD·Product code JWH·July 27, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 21, 2013

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 25, 2008

    ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEEDLE

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code FCG·December 26, 2017

    ENDOSKELETON® TCS NO 6 SWIVEL DRIVER

    FDA Adverse Event
    Malfunction ·TITAN SPINE, LLC·Product code HXX·January 28, 2016

    METASUL HD 28MM L 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·June 5, 2018

    METASUL, ALPHA INSERT, GG/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·June 5, 2018