BEUDAMED
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    COGNIS HE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CARDIOVASCULAR DIVISION·Product code NIK·September 25, 2009

    DOCUMENT PACKAGE/GSG (670G PUMP)

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZP·May 8, 2019

    AORFIX AAA FLEXIBLE STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·LOMBARD MEDICAL LTD.·Product code MIH·December 17, 2014

    AORFIX AAA FLEXIBLE STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·LOMBARD MEDICAL LTD·Product code MIH·December 17, 2014

    AORFIX AAA FLEXIBLE STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·LOMBARD MEDICAL LTD·Product code MIH·December 17, 2014

    MULTISTIX 8 SG

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JIO·May 10, 2013

    MULTISTIX 9 SG

    FDA Adverse Event
    Malfunction ·BAYER CORP. DIAGNOSTICS DIV.·Product code CFR·June 5, 1997

    *

    FDA Adverse Event
    Malfunction ·GSI INC.·Product code GDI·June 9, 2000

    GSI SPACESEAL

    FDA Adverse Event
    Malfunction ·GSI INC.·Product code GDI·June 9, 2000

    AORFIX AAA FLEXIBLE STENT GRAFT

    FDA Adverse Event
    Injury ·LOMBARD MEDICAL LTD.·Product code MIH·January 22, 2016

    BD SAFETYGLIDE¿ ALLERGY SYRINGE TRAY

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·August 23, 2023

    AM282 MANUAL AUDIOMETER W/CASE

    FDA Adverse Event
    Malfunction ·GRASON STADLER GSI·Product code ETY·December 31, 2025

    FLO-GARD 6301 DUAL CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE 9SG)·Product code FRN·January 16, 2003

    EVERSENSE SENSOR

    FDA Adverse Event
    Malfunction ·SENSEONICS INC.·Product code SBA·March 1, 2025

    MULTISTIX 8 SG REAGENT STRIPS FOR URINALYSIS

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JIR·October 6, 2017

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·January 12, 2026

    DEES DEESS GP586 PERMANENT HAIR REMOVAL DEVICE, 350,000 FLASHES HOME USE, IPL HA

    FDA Adverse Event
    Injury ·SHENZHEN GSD TECH CO., LTD·Product code OHT·July 29, 2019

    EVERSENSE SMART TRANSMITTER

    FDA Adverse Event
    Injury ·SENSEONICS INC.·Product code QHJ·April 15, 2025

    EVERSENSE TRANSMITTER

    FDA Adverse Event
    Injury ·SENSEONICS INC.·Product code QHJ·November 12, 2023

    AORFIX AAA FLEXIBLE STENT GRAFT

    FDA Adverse Event
    Death ·LOMBARD MEDICAL LTD.·Product code MIH·October 29, 2015