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

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    Filters FDA Adverse Event ×

    K-WIRE 1.1, 100MM

    FDA Adverse Event
    Malfunction ·TRIMED INC·Product code NDL·October 22, 2021

    UNK - SCREWS: 2.4 MM AND 3.0 MM HEADLESS COMPRESSION

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·June 3, 2022

    UNK - SCREWS: 2.4 MM AND 3.0 MM HEADLESS COMPRESSION

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·June 3, 2022

    TORX 8 DRIVER, 110MM NIPPLE TIP

    FDA Adverse Event
    Malfunction ·TRIMED, INC.·Product code HXX·December 4, 2024

    FOLEY CATHETER, ADULT 400 SERIES, 16 FR.

    FDA Adverse Event
    Malfunction ·MRI MEDICAL INC.·Product code KOD·January 9, 2009

    PRIMED INSTRUMENTATION INC

    FDA Adverse Event
    Malfunction ·PRIMED INSTRUMENTS INC·Product code KNW·March 26, 2002

    FOLEY CATHETER, ADULT 400 SERIES, 16 FR.

    FDA Adverse Event
    Malfunction ·MRI MEDICAL INC.·Product code KOD·December 18, 2008

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    FDA Adverse Event
    Malfunction ·MRI MEDICAL INC.·Product code KOD·November 12, 2008

    FOLEY CATHETER TEMPERATURE SENSOR

    FDA Adverse Event
    Injury ·MRI MEDICAL INC.·Product code KOD·September 19, 2007

    FOLEY CATHETER TEMPERATURE SENSOR

    FDA Adverse Event
    Injury ·MRI MEDICAL INC.·Product code KOD·May 29, 2008

    FOLEY CATHETER, ADULT 400 SERIES, 16 FR.

    FDA Adverse Event
    Malfunction ·MRI MEDICAL INC.·Product code KOD·September 18, 2008

    TRIMED TWIST DRILL

    FDA Adverse Event
    TRIMED, INC.·Product code HRS·March 30, 2012

    OMNITECH CANNULATED COMPRESSION SCREW

    FDA Adverse Event
    TRIMED, INC.·Product code HRS·March 8, 2012

    OMNITECH CANNULATED COMPRESSION SCREW

    FDA Adverse Event
    TRIMED, INC.·Product code HRS·March 8, 2012

    OMNITECH CANNULATED COMPRESSION SCREW

    FDA Adverse Event
    TRIMED, INC.·Product code HRS·March 8, 2012

    CANNCOMPSCREW 3.0MM (SELFDRILL)

    FDA Adverse Event
    Injury ·TRIMED INC·Product code HWC·April 27, 2021

    VOLAR PEG THREADED

    FDA Adverse Event
    Injury ·TRIMED INC·Product code JDS·May 6, 2021

    PEG EXTENDER

    FDA Adverse Event
    Malfunction ·TRIMED, INC·Product code LXH·December 20, 2017

    TRIMED CORTICAL BONE SCREW

    FDA Adverse Event
    TRIMED, INC.·Product code JDS·June 18, 2012

    CANNULATED TWIST DRILL

    FDA Adverse Event
    TRIMED, INC.·Product code HRS·March 8, 2012