BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    INFIMED DENTAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    HUMERAL HEAD, MANUAL DRIVER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Klassic Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 14, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2014

    UNK DEPUY CEMENT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LOD·January 7, 2011