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

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    Filters FDA Adverse Event ×

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·February 11, 2013

    UNKNOWN ZIMMER FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDI·February 23, 2011

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 LARGE TITANIUM LIGATING CL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code FZP·February 14, 2008

    OXF ANAT BRG LT XL SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·September 1, 2021

    OXF UNI CMNTLS TIB SZ D LM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·September 1, 2021

    LIGHTSHEER EC

    FDA Adverse Event
    Injury ·RH USA, INC.·Product code GEX·August 28, 2012