BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    SCIMED PM200 INFLATION MANOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sonendo GentleWave System

    FDA 510(k)
    FDA Class 2 ·Dental

    Equinoxe® Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MONOPOLAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 2, 2014

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·November 19, 2012

    SCULPTRA (POLY-L-LACTIC ACID)

    FDA Adverse Event
    Injury ·SANOFIAVENTIS U.S. LLC·Product code LMH·September 22, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018