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

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    IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1

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

    LITE SEMI-TUBULAR PLATE, 5-HOLE

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665031669·

    Durable BP Cuff

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935104957·

    SYRINGE 5ML LL SP125

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·June 10, 2019

    URETHROTOME 8667.XXX AND 8670.XXX

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

    NBX - NON-BRIDGING EXTERNAL FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COSYCOT INFANT WARMER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code FMT·May 5, 2008

    5 ML BD LUER-LOK SYRINGE STERILE, SINGLE USE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·May 8, 2019

    INRATIO

    FDA Adverse Event
    Malfunction ·ALER SAN DIEGO INC.·Product code GJS·April 10, 2013

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 18, 2011

    SERIES 7000 SANDARD TIBIA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code HSH·June 13, 2008

    Alfa Wassermann brand REF E1-8 STARLYTE III ISE Fluid Pack for use in the STARLYTE III electrolyte analyzer, Roche part number 03361152001.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·December 21, 2004