BEUDAMED
    12 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    V200 / ESPRIT

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 1, 2024

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021

    SIG MOD TIB TRAY CEM COCR 2

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code JWH·May 9, 2013

    HUDSON INCENTIVE SPIROMETER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BWF·April 13, 2011

    3.5MM SCREWDRIVER

    FDA Adverse Event
    Malfunction ·ABBOTT SPINE·Product code HXX·August 7, 2008

    SLEEK OTW PTA CATHETER

    FDA Adverse Event
    Injury ·CLEARSTREAM TECHNOLOGIES LTD.·Product code DQY·December 13, 2023