BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    STRICKLAND TRAPEZIAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RADIFOCUS GLIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

    CARDIODAY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Radifocus Glidewire Endoscopic Wire

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 9, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 6, 2011

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code MMI·July 22, 2014

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024