BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    SUTURE REMOVAL TRAY, REORDER 7950&7951

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NG-Test CARBA 5

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DRX-EVOLUTION, MODEL VX3733-SYS

    FDA 510(k)
    FDA Class 2 ·Radiology

    2008T HEMODIALYSIS SYS., WITH CDX

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·January 22, 2014

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·October 15, 2012

    CAPSURE SENSE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 10, 2010

    Basic Face Kit, Kit part numbers PS517A(B, PS517A(C, and PS517A(D. convenience custom kits used for general surgery in hospital operating room

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·October 26, 2016