BEUDAMED
    5,817 results · 49ms · 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 ×

    INTERVERTEBAL FUSION DEVICE W/BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MAX·January 8, 2015

    UNKNOWN SEPS KIT

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code ERL·May 11, 2020

    UKNOWN SEPS KIT

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code ERL·May 11, 2020

    WATCHMAN TRUSEAL ACCESS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 14, 2022

    WATCHMAN FLX LAA CLOSURE DEVICE & DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 14, 2022

    MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Death ·ABBOTT MEDICAL·Product code NKM·March 21, 2024

    MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NKM·March 21, 2024

    THERMOCOOL SMARTTOUCH SF

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·April 13, 2026

    UNK LINX MAGNETIC IMPLANT

    FDA Adverse Event
    Injury ·TORAX MEDICAL, INC.·Product code LEI·November 24, 2025

    AZURION

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 29, 2025

    CARDIOCEL

    FDA Adverse Event
    Injury ·ADMEDUS REGEN PTY LTD·Product code DXZ·November 3, 2020

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NPT·October 1, 2025

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NPT·October 1, 2025

    MITRACLIP® SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NKM·March 21, 2024

    ELEKTA SYNERGY

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·July 26, 2023

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·May 1, 2024

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·April 6, 2023

    MOSAIQ

    FDA Adverse Event
    Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·January 29, 2026

    THERAPLAN PLUS

    FDA Adverse Event
    Malfunction ·THERATRONICS INTERNATIONAL LTD.·Product code IWB·October 20, 1997

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 24, 2014