BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    CUSA Clarity Ultrasonic Surgical Aspirator System

    FDA 510(k)
    FDA Unclassified ·Unknown

    ARCH Medical Solutions - Seabrook

    FDA registration
    ARCH Medical Solutions - Seabrook·72 products·🇺🇸 United States

    RS2MI MUSCLE STIMULATOR FAMILY

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    MULTICROSS SUPPORT CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPTURE-R READY -SCREEN I AND II

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·February 17, 2012

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 1, 2024

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code HDD·August 17, 2011

    BV PULSERA REL 2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZI·July 18, 2008

    LAMITRODE 4

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, NEUROMODULATION·Product code GZB·July 9, 2013

    BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·February 14, 2024

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018