BEUDAMED
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    STROMATOLYSER-NR (L)

    FDA UDI
    SYSMEX CORPORATION·00664369000042·Lysing reagent for hematology analyzers

    LifeStyles NRL Textured Condom

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SAFESKIN PFE

    FDA Adverse Event
    Injury ·KIMBERLY-CLARK·Product code LYY·December 12, 2004

    ANSELL LIFESTYLES ULTRASENSITIVE

    FDA Adverse Event
    Other ·LMR INTERNATIONAL, INC.·Product code HIS·September 4, 2003

    SURESTEP¿ FOLEY TRAY SYSTEM BARDEX® LUBRICATH® FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·November 7, 2019

    REFLEX CATHETER

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·April 15, 2024

    SOLITAIRE RD

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·April 15, 2024

    BIOGEL

    FDA Adverse Event
    Malfunction ·MOLNLYCKE HEALTH CARE·Product code KGO·December 16, 2023

    LATEX FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZC·March 17, 2021

    PRESTIGE MEDICAL A2 ANEROID BLOOD PRESSURE UNIT

    FDA Adverse Event
    Other ·PRESTIGE MEDICAL·Product code DXN·July 3, 2014

    SURESTEP FOLEY TRAY SYSTEM 16FR, URINE METER, NRL

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code EZL·November 26, 2024

    DUODOPA_DUOPA

    FDA Adverse Event
    Injury ·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·October 17, 2025

    SALTER LABS ETCO2/O2 NASAL CANNULA #4707-13-13

    FDA Adverse Event
    Malfunction ·SUNMED HOLDINGS, LLC.·Product code CCK·September 23, 2021

    BARD MEDICAL-BARDEX LUBRICATH FOLEY CATHETER TRAY SURESTEP FOLEY TRAN SYSTEM

    FDA Adverse Event
    Other ·C.R. BARD, INC.·Product code KOD·November 18, 2015

    ELECSYS ANTI-HCV II

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MZO·September 26, 2025

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·September 20, 2019

    NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 18, 2012

    LATEX EXAM GLOVES

    FDA Adverse Event
    Other ·CARDINAL HEALTH·Product code LYY·July 25, 2003

    XPERT C. DIFFICILE BT

    FDA Adverse Event
    Malfunction ·CEPHEID AB·Product code LLH·August 11, 2025

    SOLITAIRE RD

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·April 15, 2024