BEUDAMED
    10 results · 28ms · Sources: EU EUDAMED, US FDA

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    AXSOS 3 TI LOCKING PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Logical G-Series Acetabular Shell

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215054069·

    Logical G-Series

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215006198·

    RUSCH MICROLARYNGEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UPSTREAM GR CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENTO Cup

    FDA UDI
    AMPLITUDE SAS·03701089514255·

    U-BLADE SET, TI GAMMA3 10.5X90MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 30, 2012

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·May 17, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 14, 2011