BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    THYROSCREEN TM T4 DIAGNOSTIC KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515199095·Bone File, #12A, DE, 5mm ends, 7"

    Reprocessed SoundStar 3D Diagnostic Ultrasound Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEWLIFE SCIENCES LLC, MODEL TMR

    FDA 510(k)
    FDA Class 2 ·Neurology

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 5, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 3, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 12, 2007

    Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024