BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SHEATH, 20 FR., 160 MM

    FDA Adverse Event
    Death ·TROKAMED GMBH·Product code FED·May 8, 2024

    MINI PCNL

    FDA Adverse Event
    Death ·TROKAMED GMBH·Product code FED·June 14, 2024

    COHEN INTRAUTERINE PROBE

    FDA Adverse Event
    Malfunction ·TROKAMED GMBH·Product code ---·January 4, 2006

    SHEATH, 20 FR., 130 MM

    FDA Adverse Event
    Death ·TROKAMED GMBH·Product code FED·May 8, 2024

    MINI PCNL

    FDA Adverse Event
    Death ·TROKAMED GMBH·Product code FED·June 14, 2024

    GRIP MODUL V2.0, 5-TIMES-USE MORCELLATOR SYSTEM

    FDA Adverse Event
    Malfunction ·TROKAMED GMBH·Product code HET·June 27, 2023

    MYOMA SCREW 5MM, 32CM

    FDA Adverse Event
    Malfunction ·TROKAMED GMBH·Product code MDM·July 17, 2007

    *

    FDA Adverse Event
    Other ·TROKAMED GMBH·Product code KOG·October 25, 2004

    ADAPTER FOR COHEN CANNULA

    FDA Adverse Event
    Malfunction ·TROKAMED GMBH·Product code GCJ·June 7, 2016

    GRIP MODUL V2.0, 5-TIMES-USE MORCELLATOR SYSTEM

    FDA Adverse Event
    Malfunction ·TROKAMED GMBH·Product code HET·December 5, 2023

    MYOMA SCREW 5MM, 32CM

    FDA Adverse Event
    Malfunction ·TROKAMED HENGSTLER GMBH·Product code KOG·December 5, 2003

    MYOMA SCREW 5MM, 32CM

    FDA Adverse Event
    TROKAMED HENGSTLER GMBH·Product code KOG·September 3, 2004