BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    MIST IC

    FDA 510(k)
    FDA Class 2 ·Dental

    PROPELLER HEAD SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304269774·

    DIGNITY 100

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    MIST 360 SINGLE USE APPLICATOR KIT, MIST 360 SINGLE USE APPLICATOR KIT, CASE OF 12

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

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·December 15, 2010

    AUTOLUBE-III

    FDA Adverse Event
    Malfunction ·DUPUY SYNTHES POWER TOOLS·Product code GEY·June 21, 2013

    EON RECHARGEABLE IPG, 16-CHANNEL

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2011

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·October 17, 2014