BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    450CM GUIDE WIRE FOR G.I. USE

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756375832·KNEE SCOPE PACK

    RPS ADENO DETECTOR PLUS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PROLENE (POLYPROPYLENE) 3D PATCH, NONABSORBABLE SYNTHETIC SURGICAL MESH

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

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code PGN·September 12, 2023

    MAGEC SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code PGN·September 12, 2023

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 11, 2013

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 22, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 2, 2014