BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    G7 OSSEOTI 4 HOLE SHELL 54MM F

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·August 26, 2019

    PINNACLE MULTIHOLE II CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 30, 2014

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·October 22, 2012

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·September 17, 2010

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·July 11, 2019

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 23, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·November 3, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·February 21, 2017

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·October 11, 2021

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·August 18, 2020

    G7 NEUTRAL E1 LINER 32MM F

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·August 27, 2019

    G7 NEUTRAL E1 LINER 32MM F

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PBI·August 27, 2019