BEUDAMED
    2,394 results · 67ms · Sources: EU EUDAMED, US FDA

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    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 14, 2014

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 14, 2014

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·June 28, 2016

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 30, 2014

    VARIPULSE¿ BI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code QZI·January 9, 2026

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·November 18, 2020

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·February 13, 2014

    ST JUDE AFFINITY

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL, INC·Product code DXY·March 20, 2000

    ST JUDE AFFINITY

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL, INC·Product code DXY·March 20, 2000

    ST JUDE AFFINITY

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL, INC·Product code DXY·March 20, 2000

    PROCLAIM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code GZB·September 26, 2017

    BED-CHECK ST CHAIR SENSORMAT P.N. 73030

    FDA Adverse Event
    Other ·STANLEY SECURITY SOLUTIONS, INC., SENIOR TECHNOLOGIES DIVISION·Product code KMI·July 7, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 30, 2014

    ATLAS VR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·October 1, 2002

    RIATA ST PASSIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code NVY·September 25, 2017

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·November 11, 2014

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·December 6, 2018

    JELCO PROTECTIV

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code FOZ·October 26, 2011

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·December 6, 2018

    ONX ASCENDING AORTIC 23

    FDA Adverse Event
    Injury ·ON-X LIFE TECHNOLOGIES, INC.·Product code LWQ·June 3, 2022