BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    LSP (MODEL 554) BAG MASK RESUSCITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VYGON EPIDURAL ANAESTHESIA TRAY

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DOPPLER OPTION FOR PLATINUM

    FDA 510(k)
    FDA Class 2 ·Radiology

    IBP ELBOW INTERLOK FINISH ULNAR COMPONENT STANDARD LEFT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·June 14, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·March 2, 2017

    UNKNOWN KUDO ELBOW

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDB·February 9, 2017

    CONCERTO CRT-D DR AT

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·December 13, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 14, 2014

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·December 27, 2012

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020