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

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    Filters FDA Adverse Event ×

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATIA)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·June 7, 2006

    NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·August 26, 2024

    COBAS E411 RACK SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 5, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 8, 2011

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014