BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    BD Pen Needle

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD ULTRA-FINE¿ MINI PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·January 5, 2022

    PLIF CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 25, 2014

    CAPSURE EPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·August 16, 2011

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·July 9, 2013

    KIT CONTAINING CC1.P1 AND THE IP2 INTRODUCER

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES (IRELAND) LTD.·Product code GWM·July 15, 2020