BEUDAMED
    500 results · 34ms · Sources: EU EUDAMED, US FDA

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    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    CXDI CCS NE VER.1.40.2

    FDA Adverse Event
    Malfunction ·CANON, INC·Product code MQB·May 17, 2013

    ACS HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE WIRE WITH

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DQX·August 27, 2008

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code NPT·May 11, 2016

    ESHEATH INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·December 17, 2021

    EDWARDS TF SHEATH UNKNOWN

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·October 30, 2021

    MOBI-C IMPLANT M "STANDARD" 15X17 H4.5

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MJO·April 22, 2020

    EDWARDS TRANSCATHETER TF SHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·November 20, 2018

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·October 19, 2018

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·October 19, 2018

    EDWARDS TRANSCATHETER ESHEATH

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPU·November 20, 2018

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·December 13, 2018

    EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·September 10, 2021

    PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 5, 2019

    MOBI-C P&F IMPLANT 19X19 H05

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MJO·February 4, 2020

    MOBI-C IMPLANT M"STANDARD" 15X19 H5

    FDA Adverse Event
    Malfunction ·LDR MÉDICAL·Product code MJO·July 11, 2022

    MOBI-C P&F IMPLANT 17X19 H5

    FDA Adverse Event
    Injury ·LDR MÉDICAL·Product code MJO·March 17, 2020

    MOBI-C IMPLANT; SIZE UNKNOWN

    FDA Adverse Event
    Injury ·LDR MEDICAL·Product code MJO·January 22, 2026

    MOBI-C P&F IMPLANT 13X15 H4.5

    FDA Adverse Event
    Injury ·LDR MÉDICAL·Product code MJO·May 24, 2021

    MOBI-C P&F IMPLANT 15X17 H5

    FDA Adverse Event
    Malfunction ·LDR MÉDICAL·Product code MJO·October 21, 2020