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

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    MAXISTIM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    3 TO 1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

    AlphaVent

    FDA UDI
    STRYKER CORPORATION·07613327563153·ALPHAVENT SUTURE ANCHOR 5.5MM PEEK, SUTURE ANCH...

    3-TO-1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE P

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·February 11, 2013

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    CAPITAL TEMP PUMP PROFESSIONAL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code ILO·July 24, 2014