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

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    ON*SITE ALCOHOL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    VERTESSA LITE 10 X 20CM, VERTESSA LITE 11 X 30CM

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

    CRE PULMONARY BALLOON DILATATION CATHETER, MODELS K00550300, M00550310, M00550320, M00550330, M00550340, M00550350

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·February 25, 2016

    PINNACLE DESTINATION CAROTID GUIDING SHEATH

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORP.·Product code DYB·November 2, 2010

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    VASER SYSTEM

    FDA Adverse Event
    Other ·SOUND SURGICAL TECHNOLOGIES LLC.·Product code LFL·October 12, 2006