BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    SURGISILK

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014

    Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENESECTION TRAY, ADULT 6050

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    OPERATING CYSTOSCOPE-URETHROSCOPE

    FDA Adverse Event
    Death ·KARL STORZ SE & CO. KG·Product code FGB·March 8, 2023

    MODULAR HIP

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code JDI·December 14, 2010

    MUSTANG¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LIT·February 5, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2014