BEUDAMED
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    Air Compression Therapy Device

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Contrast Line

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333207381·Contrast Line 10"(25cm) Female/Rotating Adapter...

    VETA PERITONEAL DIALYSIS CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EBONY PTA .035 PERIPHERAL DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD NEXIVA¿ DIFFUSICS¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·July 22, 2022

    NEXIVA DIFFUSICS

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 30, 2026

    PROLIEVE THERMODILITATION SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 7, 2008

    LCP-PLT 4.5/5 LE 9HO L220 TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·July 29, 2011

    PERFORMANCE PRO AMBULANCE COT

    FDA Adverse Event
    Injury ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 27, 2013

    METRX® SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HRX·October 7, 2025