BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    NORIAN REINFORCED FAST SET PUTTY/3CC

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code GXP·May 19, 2015

    ZIMMER KINECTIV MODULAR NECK

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWA·April 26, 2013

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·September 19, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 19, 2011

    HAHN TAPERED IMPLANT 4.3 X 11.5

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 15, 2022

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·December 16, 2019