BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    AMALCAP PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    VERATHON INC. BLADDERSCAN ULTRASOUND SYSTEM, MODEL BVI 9600

    FDA 510(k)
    FDA Class 2 ·Radiology

    Study Watch

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMART PERFUSION PACK: APEX MBR FMC/MID WEST REG LEXINGTON, KY

    FDA Adverse Event
    Injury ·Product code DTZ·September 11, 2007

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 22, 2024

    MULTI-LINK VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code MAF·February 28, 2013

    UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LFX·February 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014