BEUDAMED
    10 results · 25ms · Sources: EU EUDAMED, US FDA

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    MIAMI, PROTRUSIO RING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ON-Q C-BLOC

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·June 4, 2008

    YUKON OCT Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANGIOSCULPT PTA SCORING BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD SYRINGE AND NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·April 15, 2019

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 18, 2015

    28MM DIA COCR MOD HD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 15, 2014

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·October 31, 2012

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 2, 2015

    SYRINGE 10ML 21G 1-1/4IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·June 6, 2019