BEUDAMED
    6 results · 36ms · Sources: EU EUDAMED, US FDA

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    FEEDING TUBE PLACEMENT STYLET

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

    Male, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Femal, Nelaton-tip Ready-to-Use Hydrophilic Catheter; Pediatric, Nelaton-tip Ready-to-Use Hydrophilic Catheter Intermittent Catheter; Male, Tapered-Tip Tiemann Ready-to-Use Hydrophilic Catheter; Male, Olive-Tip Tiemann Ready-to-Use Hydrophilic Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    IMPLANTABLE HEART LEAD EXTENDER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 18, 2014

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·October 16, 2012

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·August 11, 2010