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

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    KENDRICK EXTRICATION DEVICE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SOLID OXYGEN SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Zimmer Biomet Select Ceramic Heads

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUADRA ASSURA CRT-D

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·April 30, 2014

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 11, 2012

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·August 3, 2010

    BiOM Rechargeable Li Ion 22.2 V Battery and BiOM Lithium Battery Charger sold as an accessory to the BiOM lower leg system: Product Number: 2001249 BiOM Battery Product Number: 2001240 BiOM Charger

    FDA Recall
    Terminated ·iwalk inc·Product code ISW·October 26, 2012