BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    OPUS 3 PULSE GENERATORS MODELS 4003,4004,4023,4024

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    PRIMAEVA MEDICAL RENESIS SYSTEM

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

    ASI Automated ASI RPR Test for Syphilis on the ASI Evolution

    FDA 510(k)
    FDA Class 2 ·Microbiology

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 18, 2014

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNEL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 26, 2010

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 20, 2012