BEUDAMED
    433 results · 38ms · 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 Status: Injury ×

    ZIPWIRE HYDROPHILIC GUIDE WIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·August 9, 2012

    PULSERIDER T, 4MM, 8MM ARCH

    FDA Adverse Event
    Injury ·PULSAR VASCULAR·Product code NJE·October 10, 2018

    PULSERIDER Y, 4MM, 8MM ARCH

    FDA Adverse Event
    Injury ·PULSAR VASCULAR·Product code NJE·October 10, 2018

    ENDURANT II EXTENSION STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·March 3, 2017

    AMPLATZER VASCULAR PLUG

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code KRD·January 14, 2016

    EMERGE MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code LIT·June 4, 2014

    TENA INTIMATES INCONTINENCE PADS

    FDA Adverse Event
    Injury ·SCA HYGIENE PRODUCTS·Product code EYQ·August 2, 2017

    SPECTRA OPTIA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code LKN·June 19, 2024

    SPECTRA OPTIA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code LKN·June 19, 2024

    SPECTRA OPTIA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code LKN·June 19, 2024

    THERMACARE MUSCLE & JOINT

    FDA Adverse Event
    Injury ·PFIZER CONSUMER HEALTH CARE·Product code IMD·October 31, 2019

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Injury ·BIOSITE INCORPORATED·Product code MMI·December 16, 2009

    AMPLATZER VASCULAR PLUG II

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code KRD·September 12, 2016

    SCEPTER MINI

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code MJN·January 9, 2021

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·March 31, 2017

    ONYX AVM

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·February 13, 2020

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·October 15, 2014

    FRED JR.

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code OUT·August 9, 2023

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·August 13, 2007

    EXPRESS LD VASCULAR

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·June 26, 2025