BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    DURACON RECESSED PATELLA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CO2RE System

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

    ANGIODYNAMICS, INC., MICRO ACCESS KITS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    URETEROSCOPE, 8,6/9,8 FR. X 430 MM, 7°, 6,4 FR. CHANNEL, WITH A0396

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FGB·December 16, 2016

    REVO MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LWP·February 9, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 6, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014