BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    STRYKER PNEUMO SURE INSUFFLATION TUBING

    FDA Adverse Event
    Malfunction ·STRYKER CORP·Product code HIF·March 27, 2019

    TESS GLENOID REVERSE HEAD DIAMETER 36

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·February 2, 2007

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 8, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·March 22, 2011

    PREMIUM SURGICLIP S-9.0 TITANIUM

    FDA Adverse Event
    Malfunction ·PONCE - USS·Product code GDO·May 8, 2008

    VGXP XP E1 TIB BRG RL 9X79

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·October 8, 2018

    VGXP XP E1 TIB BRG RM 9X79

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·October 8, 2018

    VGXP INTLK FEMORAL RT 70

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·October 8, 2018