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

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    Introcan Safety® 2 IV Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEXUS PAV LUER LOCK DEVICE, MODEL NIS-4

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Portable Electro-Stimulation Therapy Device, Model: LGT-232(US)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BD VACUTAINER® K2E 3.6MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 11, 2024

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 10, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·July 22, 2013

    BD VACUTAINER ECLIPSE BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·January 15, 2020