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

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    Filters FDA Adverse Event ×

    12/14 ARTICUL 40MM M SPEC+8.5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. 8010379·Product code LPH·March 20, 2013

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FRN·March 4, 2011

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 15, 2014

    EVIS LUCERA COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·May 1, 2023

    UNKNOWN HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·May 13, 2021

    UNKNOWN GLENOID

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·May 13, 2021