BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    RIASSIST RAST DATA REDUCTION/QUALITY

    FDA 510(k)
    FDA Class 2 ·Immunology

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127020988·Parabolic Reamer 70mm

    REUSABLE SMARTSTITCH SUTURE DEVICE, MODELS OM-8007, OM-8500

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

    EXSPIRON 1XI

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARGYLE SALEM SUMP TUBE WITH ANTI-REFLUX VALVE

    FDA Adverse Event
    Malfunction ·SHERWOOD DAVIS AND GECK·Product code KNT·August 29, 1996

    UNK ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·March 26, 2014

    NEUROMONICS OASIS TINNITUS TREATMENT

    FDA Adverse Event
    Injury ·NEUROMONICS·Product code KLW·November 6, 2012

    1600 SEMI AUTOMATIC DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 1, 2010