BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Everyway OTC EMS, Model EV-805

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SAPIENS TIP CONFIRMATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROSPERA OTC TENS ELECTRONIC PULSE MASSAGER

    FDA 510(k)
    FDA Class 2 ·Neurology

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·October 24, 2019

    PAINSMART

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    CAPSURE SP NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTB·July 14, 2011

    CENTRA 850 BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 8, 2008

    VARIABLE SELF-DRILLING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·October 4, 2017