BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    STERI-PAK LF BOWIE-DICK TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SARNS WIRE-REINFORCED VENOUS RETURN CAN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NeuroShield

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEGASUTURECUT NEEDLE DRIVER

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·March 5, 2013

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·August 7, 2014