BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Ultiri Measurement System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777457·LUMBAMED PLUS FLEX PAD WM SILVER III

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777600·LUMBAMED BASIC DORSAL STAY WM SILVER III

    NEXT Fine Wintergreen Prophy Paste Box 200

    FDA UDI
    Preventech·D024220243·NEXT Fine Wintergreen Prophy Paste Box of 200 2...

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·August 28, 2020

    GAM-200

    FDA 510(k)
    FDA Class 2 ·Dental

    LASERPRO 16

    FDA 510(k)
    FDA Class 2 ·Radiology

    T:SLIM X2 INSULIN PUMP

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code LZG·February 14, 2020

    NOVA MAX GLUCOSE MONITOR

    FDA Adverse Event
    Other ·NOVA BIOMEDICAL CORP.·Product code NBW·October 31, 2008

    8 CHANNEL, TRIAL, 60 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 16, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013