BEUDAMED
    10 results · 36ms · Sources: EU EUDAMED, US FDA

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    RX LENS SERIES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    MONITOR, NEONATAL, MODEL 78260A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634, 5M9693

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 18, 2007

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 28, 2012

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·December 30, 2013

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 25, 2024

    SENTRANT INTRODUCER SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code DYB·September 6, 2024

    PIPELINE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·December 18, 2024

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·December 9, 2024