BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HALO AP Dx

    FDA 510(k)
    FDA Class 2 ·Pathology

    MYOSYSTEM WITH CUSTOMIZING

    FDA 510(k)
    FDA Class 2 ·Neurology

    ULTRA RENEW PLUS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD 1ML SYRINGE LUER-LOK TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 29, 2020

    AMS GREENLIGHT HPS FIBER

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·March 9, 2015

    BD 1ML SYRINGE LUER-LOK TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·August 4, 2020

    CAPSUREEPI

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTB·November 6, 2014

    3002 SECURE II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 19, 2011

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 18, 2013

    BD SYRINGE LUER-LOK TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 25, 2020