BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    DIAGNON FERRITIN 125 I RIA KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    SURETEMP PLUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RETRACTION PASTE

    FDA 510(k)
    FDA Unclassified ·Unknown

    CAPTIFLEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code FDI·May 23, 2014

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 13, 2012

    DURATA STS OPTIM ACTIVE FIXATION, SJ4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 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