BEUDAMED
    44 results · 24ms · Sources: EU EUDAMED, US FDA

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    SBI CARPAL FUSION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA UDI
    FX SOLUTIONS·03701037313503·STABILITY TRIAL CUP FOR BOACH Ø32+3 STANDARD TR...

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111154157·SCALPEL HDL #3

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180501306·Medial/Lateral Angled LIF Curette - SIZE 3, LEFT

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180501313·Medial/Lateral Angled LIF Curette - SIZE 3, RIGHT

    ANSPACH ANGLED MICRONOSE ATTACHMENT

    FDA 510(k)
    FDA Class 2 ·Neurology

    CHILLBUSTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·June 18, 2019

    ABBVIE NJ

    FDA Adverse Event
    Death ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·October 30, 2015

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·November 26, 2018

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·July 13, 2018

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE MEDICAL DEVICE CENTRE·Product code KNT·October 11, 2017

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·September 11, 2018

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·January 3, 2019

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·October 22, 2018

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·January 27, 2026

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE MEDICAL DEVICE CENTRE·Product code KNT·January 26, 2017

    ABBVIE NJ

    FDA Adverse Event
    Death ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·September 6, 2018

    ABBVIE NJ

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·April 26, 2018

    ELECTRIC PEN DRIVE 90,000 RPM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·April 17, 2013