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

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    Vista Clear

    FDA 510(k)
    FDA Unclassified ·Unknown

    Reveal

    FDA UDI
    Oticon A/S·05707131341693·G20, BTE 13 2.4G 85 C063 REVEAL

    TRUCLEAR INCISOR PLUS BLADE 2.9

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CSI MODEL 5K MANAGED HEALTH SYSTEM KIOSK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MIRU 1DAY UPSIDE (MIDAFILCON A)

    FDA Adverse Event
    Injury ·MENICON CO., LTD.·Product code LPL·January 22, 2025

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 7, 2008

    UNKNOWN DEPUY SZ 2.5 TIBIAL TRAY

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 27, 2013

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·July 29, 2011