BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    INTRA-VIEW BILATERAL TRANSCRANIAL DOPPLER DEVICE, SMART-LITE PORTABLE BILATERAL TRANSCRANIAL DOPPLER DEVICE, COMPACT MOD

    FDA 510(k)
    FDA Class 2 ·Radiology

    AUTO SUTURE(R) MODIFIED ENDOSCOPIC LIGATING LOOP

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

    GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE

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

    PSO KNEE BONE SUBSTITUTION

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

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GWM·January 31, 2017

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GWM·January 31, 2017

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GWM·December 16, 2016

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·April 20, 2016

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·April 20, 2016

    PSO KNEE BONE SUBSTITUTION

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

    SYNCARDIA CIRCULATORY SUPPORT SYSTEM CONSOLE

    FDA Adverse Event
    Malfunction ·SYNCARDIA SYSTEMS, INC.·Product code LOZ·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

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·April 20, 2016