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

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    TECNIS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·May 15, 2019

    TECNIS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·May 15, 2019

    ALERE DETERMINE HIV 1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·December 6, 2022

    DETERMINE HIV-1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·March 14, 2025

    ALERE DETERMINE HIV 1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·December 6, 2022

    DETERMINE HIV-1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·March 14, 2025

    PROLENE SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·April 30, 2026

    ENTERPRISE 5000

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH POLSKA SP Z O.O·Product code FNL·January 4, 2017

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 9, 2022

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code KYF·September 9, 2020

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code KYF·September 9, 2020

    SONATA TRANSCERVICAL FIBROID ABLATION SYSTEM

    FDA Adverse Event
    Injury ·GYNESONICS·Product code KNF·September 3, 2025

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 12, 2022

    BLAKE DRAIN UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GBX·September 8, 2022

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DTQ·September 6, 2011

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·December 19, 2024

    MENTOR - SILTEX

    FDA Adverse Event
    Malfunction ·MENTOR HS, INC.·Product code FWM·October 8, 2003

    MENTOR, SALINE BREAST IMPLANTS

    FDA Adverse Event
    Injury ·MENTOR/HS, INC.·Product code FWM·June 24, 2009

    MENTOR

    FDA Adverse Event
    Other ·MENTOR HS, INC.·Product code FTR·January 22, 1997

    MENTOR

    FDA Adverse Event
    Malfunction ·MENTOR HS, INC.·Product code FWM·January 22, 1997