BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SULOX, HEAD, M, 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·May 31, 2018

    AVENIR MUELLER, STEM, STANDARD, UNCEMENTED, HA, 4, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·May 31, 2018

    DURASUL, ALPHA INSERT, HH/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·May 31, 2018

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·June 10, 2014

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 7, 2010

    PONTO WIDE IMPLANT WITH ABUTMENT

    FDA Adverse Event
    Other ·OTICON MEDICAL AB·Product code MAH·November 23, 2012

    ALLOFIT ALLOCLASSIC SHL 50/HH

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·May 31, 2018