BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    OCULAR RESPONSE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ADMIRA FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    LUNAR REPORT GENERATOR II

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD ULTRA FINE PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code FMI·January 17, 2020

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 10, 2023

    UNK GEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·November 14, 2018

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·April 29, 2013

    SM104 MSERIES W5TH WHL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·April 13, 2011

    PUMP MMT-722NAP PRDGM INS V2.2 PL EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·July 18, 2008

    BD ULTRA FINE PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 25, 2020