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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    AFFIRM VPIII MICROBIAL IDENTIFICATION TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    TEMPUS(TM) CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BESMED VARIOUS MODELS OF TENS, BE-550/BE-660

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRANSPAL DISTRACT BODY 16-24

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code MQN·January 28, 2013

    ZIMMER.COM

    FDA Adverse Event
    Injury ·Product code JDI·December 7, 2010

    HOMES

    FDA Adverse Event
    Malfunction ·SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTIONS·Product code KFZ·April 8, 2014