BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LEEP SYSTEM 1000 ESU GEN

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·October 29, 2020

    COOPERSURGICAL

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code ITX·April 29, 2026

    SMR CEMENTLESS MINI STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·January 20, 2021

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code CEM·March 26, 2026

    3DKNEE

    FDA Adverse Event
    ENCORE MEDICAL, L.P.·Product code JWH·March 12, 2013

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC EUROPE SARL·Product code MHY·February 17, 2011

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 14, 2008

    EVIS EXERA III XENON LIGHT SOURCE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·March 13, 2024