BEUDAMED
    9 results · 29ms · Sources: EU EUDAMED, US FDA

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    LOGIQ P9 and LOGIQ P7

    FDA 510(k)
    FDA Class 2 ·Radiology

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·January 14, 2026

    WIRELESS/WIRED FDR D-EVO FLAT PANEL DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    PERIOGLAS PUTTY-BIOACTIVE BONE GRAFT GEL

    FDA 510(k)
    FDA Class 2 ·Dental

    PUMP CADD LEGACY

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·January 18, 2022

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·March 4, 2015

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 11, 2013

    US ELITE SYSTEM CYSTOURETHROSCOPE SHEATH

    FDA Adverse Event
    Other ·GYRUS ACMI, INC.·Product code FBO·June 6, 2011

    ITREL II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 17, 2008