BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ROUND FILTER POLYPROVPYLENE

    FDA Adverse Event
    Malfunction ·SPS MEDICAL SUPPLY CORP·Product code FRG·June 25, 2013

    MECTALIF TRANSFORAMINAL INTERBODY FUSION DEVICE 12X30X8 L°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·September 14, 2018

    LUMENIS

    FDA Adverse Event
    Injury ·LUMENIS INC.·Product code GEX·May 8, 2013

    VPAP SV

    FDA Adverse Event
    Death ·RESMED LTD.·Product code MNS·May 27, 2011

    ACCU-CHEK ACTIVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 13, 2008

    BONE PIN, 3.2 X 80 MM, STERILE (2 PACK)

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·October 24, 2015

    BONE PIN- 3.2 X 80 MM- STERILE (2 PACK)

    FDA Adverse Event
    Injury ·MAKO SURGICAL CORP.·Product code OLO·June 25, 2015

    BONE PIN, 3.2 X 80 MM, STERILE (2 PACK)

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 17, 2015

    BONE PIN- 3.2 X 80 MM- STERILE (2 PACK)

    FDA Adverse Event
    Injury ·MAKO SURGICAL CORP.·Product code OLO·June 9, 2015