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

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    BIPOLAR HIP DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ISY

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO LAPAROSHIELD CONDITIONED INSUFFLATION SET

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

    TOTAL ASR ACET IMP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 27, 2014

    TI COLLAR FOR 6MM DUAL-OPENINGIMPLANTS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·November 15, 2012

    OPTEASE RETRIEVABLE VENA CAVA FILTER - 55CM-EU

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code DTK·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