BEUDAMED
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    MILTEX RIGID STERILIZATION CONTAINER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074195315·PROXIMAL SCREW 5.5 X 70, TI

    IBP_CO_AG Module(with 02)(FDA)II

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904098470·

    BREAST IMMOBIIZATION AND BIOPSY DEVICE MR-BIOPSY 160

    FDA 510(k)
    FDA Class 2 ·Radiology

    BLUE MAX BALLOON DILATATION CATHETER, MAXFORCE BALLOON CATHETER, XXL BALLOON DILATATION CATHATER, SYMMETRY BALLOON DILA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLIP

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL, INC.·Product code MND·March 12, 2013

    FLAIR ENDOVASCULAR STENT GRAFT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code MIH·March 15, 2011

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

    Inflation Kit. Label reads in part: ''CUSTOM KIT...MERIT MEDICAL''. Latex free, Sterile if package is unopened or undamaged. Part Numbers: K05-00122H, K05-50031D, K0510570, K05-01536A, K05-01153C, K05-00276C, K05-0019313, K05-00077F, K05-01296A, K05-00134D, K05-01676, K05-01250, K05-00800, K05-01545, K05-00819, K05-01069C, K05-00559F, K05-50078B, K05-00116C, K05-00459C, K05-01290A,K05-01146, K05-50054D, K05-00946B, K05-00203K, K05-00682B, K05-YSI008A, K05-YPI011, K05-00746, K05-003139, K05-00751G,K05-00180G, and K05-00553F.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc·Product code DQO·October 1, 2003