BEUDAMED
    10 results · 41ms · Sources: EU EUDAMED, US FDA

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    K090539

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·February 26, 2026

    BE-VKMO 70000 #QUADR-I HMO70000+VHK7100

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

    BE-VKMO 70000 #QUAD-I HMO70000+VHK7100

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

    BE-VKMO 70000 #QUADR-I HMO70000+VHK7100

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

    ECHO B-MTRC MP FP HO 9

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·April 5, 2022

    BE-VEMO 7000 #QUADR-I HMO70000+VHK7100

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·May 2, 2013

    FREESTYLE

    FDA Adverse Event
    Injury ·Product code LFR·September 15, 2014

    ALARIS PUMP MODULE IV ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·April 19, 2011

    LOGIC CC TIB INSERT SIZE 2, 21MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 9, 2024