BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    SYNTHES RESORBABLE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·November 2, 2012

    SPECIFIC IGE EIA-TURBO ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    ENVICLUSIVE (TM)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PSO KNEE BONE SUBSTITUTION

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022

    PSO KNEE BONE SUBSTITUTION

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019

    DISPOSABLE HEMOSTASIS CLIP

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC.·Product code MND·January 29, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 31, 2025