BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    PHARMA-PLAST CONNECTING TUBE TYPE SUCT-

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Fix2Lock (PEEK Self Punching)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Diazyme Fibrinogen Assay, Diazyme Fibrinogen Calibrator Set, Diazyme Fibrinogen Control Set

    FDA 510(k)
    FDA Class 2 ·Hematology

    TRILOGY SHELL WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MEH·November 15, 2012

    GEMSTAR 7 THERAPY IN

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 14, 2014

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·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