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

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    Filters Regulation: Us FDA ×

    ACORN ANTERIOR/POSTERIOR COMPOSITE RESTORATIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665584076·MIS Cannulated Screw, Ø10.5 x 65mm, Ø6.0mm Rod

    CONDYLAFORM II NFC

    FDA 510(k)
    FDA Class 2 ·Dental

    Fully Automatic Electronic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMPLANT HOLDER FOR SYNFIX(TM)-LR

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code LXH·February 14, 2013

    CARPENTIER-EDWARDS BIOPROSTHETIC VALVED CONDUIT

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·January 13, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 28, 2014