BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    MEDPOR ATTRACTOR MAGNETIC COUPLING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HARRISON HAND HELD ADJUSTING INSTRUMENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    PSYCHEMEDICS ANALYSIS OF MORPHINE IN HAIR

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    AGILTRAC .018 PERIPHERAL DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code LIT·June 26, 2008

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 8, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 22, 2011

    CIDEX PLUS 28 DAY SOLUTION

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON·Product code LRJ·May 9, 2008

    M2A-MAGNUM 42-50MM TPR INSRT-3

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 19, 2013

    M2A-MAGNUM 42-50MM TPR INSRT-6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 19, 2013

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 19, 2013

    M2A-MAGNUM PF CUP 52ODX46ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 19, 2013

    TAPERLOC POR FMRL 9X137

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MEH·November 19, 2013

    M2A-MAGNUM PF CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·September 24, 2013