BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    COOK TEST TUBE HEATER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    KFX PEEK BONE ANCHOR WITH PRE-ATTACHED SUTURES AND INSERTER HANDLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COULTER® AC *T DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·February 28, 2013

    CARBOFLO VASCULAR GRAFT

    FDA Adverse Event
    Death ·BARD PERIPHERAL VASCULAR, INC.·Product code DYF·February 2, 2011

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·August 6, 2014