BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    MAXILUBE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LENSAR Laser System - fs 3D

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HOLTER RECORDER H3+

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 18, 2013

    TUBE, ENDOTRACHEAL HVLP CUFF M

    FDA Adverse Event
    Other ·MEDLINE INDUSTRIES, INC.·Product code BTR·December 21, 2010

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 17, 2014