BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    APEX OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACUVUE OASYS (senofilcon A) with Photochromic Additive

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    RESPIFIT S, MODEL RS-LR1001004

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TRUERESULT

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code LFR·June 5, 2014

    2520274-2013-10707

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code MNI·February 22, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·February 2, 2011

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015