BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    CANDELA FAMILY OF PULSE DYE LASER SYSTEMS

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

    CT LUCIA

    FDA UDI
    CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100942·3-piece, monofocal, hydrophobic, acrylic, intra...

    ARTHREX FIBERWIRE, MODEL SPU-02NB-3800

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

    HYSTEROSCOPE OPERATING SHEATH AND INSERT, MODEL 8988.031/.041/.231/.241

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HEMICAP/UNICAP RESURFACING PROSTHESIS

    FDA Adverse Event
    Other ·ARTHROSURFACE, INC.·Product code HSD·December 7, 2012

    FOUNDATION KNEE

    FDA Adverse Event
    ENCORE MEDICAL, L.P.·Product code JWH·April 10, 2013

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·April 12, 2011

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·May 27, 2008

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·June 25, 2025