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

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    CIOS ALPHA

    FDA 510(k)
    FDA Class 2 ·Radiology

    NexxZr™ T / D-100-20-NT-B400-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113047·

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981204556·Trial, 11mm x 32mm x 9mm, 5 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981190408·Interbody, 11mm x 32mm x 9mm, 5 Deg

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981288754·Interbody, 11mm x 32mm x 9mm, 5 Deg, 3D

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PASSMED SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·August 31, 2018

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·May 29, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 16, 2011

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code MIH·August 21, 2008