BEUDAMED
    45 results · 66ms · Sources: EU EUDAMED, US FDA

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    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DXF·December 21, 2022

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL CO., INC.·Product code DXF·April 30, 2014

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL CO., INC.·Product code DXF·June 26, 2014

    VERSACROSS TRANSSEPTAL SHEATH

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code DYB·May 14, 2021

    BMC RF CANNULA

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GXI·April 5, 2012

    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL CO., INC.·Product code DQX·May 10, 2012

    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA Adverse Event
    Death ·BAYLIS MEDICAL CO., INC.·Product code DQX·May 25, 2007

    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA Adverse Event
    Death ·BAYLIS MEDICAL CO., INC.·Product code DQX·May 25, 2007

    BMC RADIOFREQUENCY PUNCTURE GENERATOR

    FDA Adverse Event
    Other ·BAYLIS MEDICAL CO., INC.·Product code GEI·June 29, 2007

    POWERWIRE RADIOFREQUENCY GUIDEWIRE

    FDA Adverse Event
    Death ·BAYLIS MEDICAL CO., INC.·Product code DQX·May 25, 2007

    BAYLIS PAIN MANAGEMENT GENERATOR PMG-115-TD

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GEI·December 7, 2018

    SINERGY COOLED RADIOFREQUENCY PROBE

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GXI·March 18, 2013

    COOLED RF PERISTALTIC PUMP CONNECTOR CABLE

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GEI·March 18, 2013

    NRG TRANSSEPTAL NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL CO., INC.·Product code DRC·March 17, 2014

    TRANSDISCAL PROBE KIT

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GEI·February 28, 2014

    RADIOFREQUENCY PROBE-CURVED

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GXI·January 7, 2014

    NEEDLE

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL CO., INC.·Product code DXF·August 12, 2023

    TORONTO TRANSSEPTAL CATHETER

    FDA Adverse Event
    Injury ·BAYLIS MEDICAL CO., INC.·Product code DXF·April 14, 2009

    MULTI-RADIOFREQUENCY CABLE

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GXI·April 3, 2013

    MULTI-RADIOFREQUENCY CABLE

    FDA Adverse Event
    Malfunction ·BAYLIS MEDICAL CO., INC.·Product code GXI·May 24, 2013