BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESIS

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

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 14, 2024

    Sapphire NC Plus Coronary Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VANGUARD REPROCESSED PULSE OXIMETER SENSORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MPS DISPOSABLE

    FDA Adverse Event
    Malfunction ·QUEST MEDICAL, INC.·Product code DTR·May 13, 2014

    PINN CAN BONE SCREW 6.5MMX20MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS, INC·Product code NDJ·November 2, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 12, 2013