BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    16 X 125 MM TEST TUBE, CATALOG #01-401

    FDA 510(k)
    FDA Class 1 ·Hematology

    POWDER FREE SYNTHETIC NITRILE NEOPRENE EXAMINATION GLOVES, SIZES SMALL,MEDIUM, LARGE, AND X-LARGE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SpassageQ

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® SINGLE USE HOLDER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·December 6, 2017

    OPTIVANTAGE DH

    FDA Adverse Event
    Injury ·LIEBEL-FLARSHEIM CO.·Product code DXT·January 22, 2013

    COAGUCHEK® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·December 16, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 11, 2014

    PRESCRIPTIVE OXY PACK - CAPIOX

    FDA Adverse Event
    Injury ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·April 30, 2018