BEUDAMED
    815 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·August 11, 2014

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·August 24, 2022

    EMERGE?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·June 25, 2014

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·February 25, 2014

    BD SYRINGE 50CC LL TIP CONVENIENCE PAK

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMF·November 7, 2023

    THERMACARE NECK, SHOULDER & WRIST

    FDA Adverse Event
    Malfunction ·PFIZER CONSUMER HEALTH CARE·Product code IMD·October 31, 2019

    DVI SCA-EX

    FDA Adverse Event
    Malfunction ·DEVICES FOR VASCULAR INTERVENTION·Product code MCX·September 21, 1994

    SCA EPIDURAL INTRODUCER

    FDA Adverse Event
    Malfunction ·EPIMED INTERNATIONAL·Product code BSO·October 5, 2004

    SCA - EX ATHEROCATHETER

    FDA Adverse Event
    Malfunction ·DEVICES FOR VASCULAR INTERVENTION·Product code MCX·January 19, 1993

    UNKNOWN_MEDICAL - BELFAST_PRODUCT

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·April 7, 2021

    HEARTSINE SAMARITAN 500P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·August 18, 2015

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·January 23, 2014

    HEARTSINE SAMARITAN 300P AND PAD-PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·November 5, 2020

    THERMACARE NECK, SHOULDER & WRIST

    FDA Adverse Event
    Malfunction ·PFIZER CONSUMER HEALTH CARE·Product code IMD·November 13, 2020

    THERMACARE NECK, SHOULDER & WRIST

    FDA Adverse Event
    Malfunction ·PFIZER CONSUMER HEALTH CARE·Product code IMD·September 6, 2019

    PACKAGE,500P,PP03,USB,EN,500-BAS-CN-10

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·July 16, 2018

    RAPIDPOINT 500 BLOOD GAS ANALYZER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code CHL·December 26, 2019

    SCA-EX ATHEROCATH, 7FR

    FDA Adverse Event
    Malfunction ·DEVICES FOR VASCULAR INTERVENTION, INC.·Product code MCW·February 25, 1994

    SCA-EX ATHERECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·GUIDANT ACS/DVI·Product code MCX·September 10, 1997

    SCA-EX ATHERECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·GUIDANT ACS/DVI·Product code MCX·August 21, 1997