BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    RADIONICS MICROELECTRODE KIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517199768·MaXcess-C Arm, Assem Secondary

    ACU-ALERT

    FDA 510(k)

    BIOLOX CONTOURA Ceramic Femoral Head

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STERRAD 100S STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 8, 2006

    SROM STM STD 36+12L 15X20

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 6, 2013

    DEXATIP

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTB·February 15, 2011

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    STERRAD 100NX STERILIZER 1-DR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 6, 2021