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

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    EMIT QST PHENOBARBITAL ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Legacy™2 Implant

    FDA UDI
    IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307101741·Ø4.2 x 16 Platform 3.5mmD

    COMMAND ULTRA II

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    DORC COMPACT MICRO SURGICAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 28, 2014

    LEAD MODEL 304

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·November 15, 2012

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·September 14, 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