BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    INNOVASIVE ROCLET BONE TUNNEL AUGMENTATION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970423·anteriors; shade D3; mould ITM

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295250401·SIGMA TIBIAL INSERT FIXED BEARING CURVED PLUS 1...

    TR BAND

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DentureID Microchip

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·February 20, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·January 18, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code ITI·July 31, 2014