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

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    NUCAMMA RX

    FDA 510(k)
    FDA Class 2 ·Radiology

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982045·posteriors; shade B1; size M; lower jaw

    Lotus III Multi-Pulsed Er: Yag Laser System

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

    MODIFICATION TO MCARE 300 VITAL SIGNS MONITOR, MODEL 91220

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IMP CBL DIA2 SS CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016

    IMP CBL DIA2 SS CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016

    IMP CBL DIA2 SS &CABLE SLEEV

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 30, 2016

    IMP CBL DIA2 SS & CABLE SLEEVE

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code JDQ·July 20, 2016

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    FDA Adverse Event
    ABBOTT LABORATORIES, INC.·Product code HQL·February 18, 2013

    UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LGD·February 8, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 5, 2014