BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event × Regulation: Us FDA × Clear all

    STOCKERT CORONARY PERFUSION CANNULAE

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DWF·March 7, 2019

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·March 27, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·March 17, 2011

    APEX FLEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·March 26, 2008

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023

    FALLOPIAN TUBE OCCLUSION INSERT

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 3, 2023