BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GENESIS II LONG STEM 10MMX70MM

    FDA Adverse Event
    Injury ·SMITH AND NEPHEW, INC.·Product code JWH·October 2, 2018

    JOURNEY TIBIA BASE NP LT SZ 4

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 2, 2018

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·April 24, 2023

    T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 25, 2025

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIM·August 15, 2011

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·October 29, 2008

    PINN MAR +4 10D 28IDX46OD

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·July 9, 2013

    INJECTOR N35-O

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code ONB·March 18, 2024