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

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    LEUKOFIX POROS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    BEHIND-THE-EAR HEARING INSTRUMENT, H54

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    MESH GPS - LARGE, SMALL, SM, SM SMALL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ENDOTRACHEAL TUBE 8229307 NIM EMG 7MM RE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ETN·May 6, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 16, 2012

    ACRYSOF IQ RESTOR SINGLEPIECE IOL

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. - HUNTINGTON·Product code MFK·May 22, 2015

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018