BEUDAMED
    8 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Paltop Short Implants

    FDA 510(k)
    FDA Class 2 ·Dental

    SPINEFRONTIER LESPLASTY POSTERIOR CERVICAL LAMINOPLASTY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Klassic Knee System Tibial Inserts, PS-Max

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·March 30, 2018

    MTS A/B/D MONOCLONAL GROUPING CARD

    FDA Adverse Event
    Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 14, 2008

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INT'L., LTD·Product code KWA·August 18, 2011

    DIMENSION XPAND PLUS W/ HM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JGS·July 18, 2013

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·April 3, 2018