BEUDAMED
    7 results · 21ms · 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

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDI·June 5, 2014

    M PROFILE PLATE, T-SHAPE, 90 DEGREES NARROW, 6 HOL

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER GMBH & CO. KG·Product code HRS·November 12, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 29, 2010

    BD DISC CEFTAZIDIME CAZ-30 JAPAN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code JTN·January 18, 2022

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DYB·May 4, 2018

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

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