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

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    CereLink ICP Monitor, CereLink ICP Extension Cable

    FDA 510(k)
    FDA Class 2 ·Neurology

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304271005·

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304472891·

    N/A

    FDA UDI
    Ortho Development Corporation·00822409131457·Asymmetric Tibial Tray Sizing Template Size 6

    AQUASIL ULTRA SMART WETTING IMPRESSION MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    MICROCOOL BREATHABLE HIGH PERFORMANCE SURGICAL GOWNS

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

    I-STAT EC4+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

    I-STAT EC4+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

    I-STAT EC4+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

    I-STAT EC4+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

    I-STAT EC4+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·June 16, 2025

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·June 16, 2025

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·October 22, 2025

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·February 12, 2025

    OT VERIO SYNC METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    CARDIOCHEK PLUS ANALYZERQ

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·August 18, 2022

    CARDIOCHEK PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·PTS DIAGNOSTICS·Product code CGA·July 28, 2023