BEUDAMED
    25 results · 23ms · Sources: EU EUDAMED, US FDA

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    KEMTROL SERUM CONTROL-ABNORMAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    N/A

    FDA UDI
    PENTAX OF AMERICA, INC.·04961333242320·CABLE,3.5MM TO 3.5MM MONO PLUG

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123120·K-WIRE - DOUBLE TROCAR 0.9mm DIA x 150mm

    EXTENSION SET, MODELS 1911-512

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDOBEAM HOLMIUM LASER FIBERS

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

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 130

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 17, 2012

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 17, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·December 13, 2010

    ELLIPSE VR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 8, 2014

    UNKNOWN COMPREHENSIVE REVERSE GLENOSPHERE

    FDA Adverse Event
    Death ·BIOMET ORTHOPEDICS·Product code KWS·August 3, 2017

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HSD·August 3, 2017

    UNKNOWN GLENOSPHERE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·August 3, 2017

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HSD·August 3, 2017

    UNKNOWN COMPREHENSIVE HEMI-ARTHROPLASTY STEM

    FDA Adverse Event
    Death ·BIOMET ORTHOPEDICS·Product code HSD·August 3, 2017

    UNKNOWN TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HSD·August 3, 2017

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·August 3, 2017

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HSD·August 3, 2017

    UNKNOWN COMPREHENSIVE HUMERAL HEAD

    FDA Adverse Event
    Death ·BIOMET ORTHOPEDICS·Product code KWS·August 3, 2017

    UNKNOWN COMPREHENSIVE REVERSE GLENOID BASEPLATE

    FDA Adverse Event
    Death ·BIOMET ORTHOPEDICS·Product code KWS·August 3, 2017

    UNKNOWN BASEPLATE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·August 3, 2017