BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    3008261720-2024-002557

    FDA Adverse Event
    Injury ·JJGC INDUSTRIA E COMERCIO DE MATERIAIS DENTARIOS SA·Product code DZE·September 2, 2024

    RHK SEGMENTAL SHORT YOKE

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·December 7, 2016

    QUICKSET TPRD HEX SCDR U-JOINT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·June 26, 2014

    QUICKSET TPRD HEX SCDR U-JOINT

    FDA Adverse Event
    Malfunction ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LXH·June 13, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·February 15, 2013

    MERIT CUSTOM KIT

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DQO·January 28, 2011

    INDURA

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·February 8, 2008

    QUICKSET TPRD HEX SCDR U-JOINT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·March 22, 2014

    QUICKSET TPRD HEX SCDR U-JOINT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·July 28, 2014