BEUDAMED
    8 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    APTIMA COMBO 2 ASSAY

    FDA Adverse Event
    Injury ·HOLOGIC, INC.·Product code LSL·December 5, 2024

    INTEGRAL/X POR RED PROX 13MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·July 18, 2019

    ROTICULATOR ENDO GRASP* 5MM W/SPIN LOCK

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC PUERTO RICO INC·Product code GET·July 9, 2015

    6600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 6, 2014

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·November 9, 2009

    SELEX/MAGNUM MOD HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 24, 2018

    FEMORAL MODULAR HEAD - S Ø28MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·April 13, 2023

    PECTUS SYSTEM JANTON 12" TI PECTUS BAR 3.048CM (12") (L) TITANIUM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 2, 2019