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

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    ICONN Answer II Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WELCH ALLYN SPOT VITAL SIGNS LXI MODEL 45000 SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NUCLEUS-X, MODEL 230X

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EPIX UNIVERSAL CLIP APPLIER

    FDA Adverse Event
    APPLIED MEDICAL·Product code FZP·December 7, 2012

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Injury ·BD MEDICAL (BD EAST) PHARMACEUTICAL SYSTEMS·Product code FMI·March 16, 2016

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·July 27, 2017

    TENDRIL ST

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·July 27, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 14, 2013

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 30, 2008

    HEARTWARE VENTRICULAR ASSIST SYSTEM- PUMP

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·October 16, 2018

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·August 25, 2017