BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    extriCARE 2400 NPWT System with extriCARE 2400 NPWT Pump and extriCARE NPWT Foam Dressing Kit

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    REMINGTON I-LIGHT HAIR REMOVAL SYSTEM

    FDA Adverse Event
    Injury ·SHASER INC·Product code ONF·May 21, 2021

    ROBERTSITE VIAL ADAPTER, MODEL 245700021

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNTHES MATRIX SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    1024879-2017-01085

    FDA Adverse Event
    Malfunction ·December 1, 2017

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 31, 2013

    HEARTSTART MRX - EMS DEFBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·June 16, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 3, 2008