BEUDAMED
    7 results · 28ms · 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 ×

    MODEL 1309 AUDIO MONITOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515205949·Screwdriver, single slot

    DEVON ACCUBP CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RT Elements, Cranial SRS, Spine SRS, Multiple Brain Mets SRS, RT QA, Adaptive Hybrid Surgery Analysis, Dose Review

    FDA 510(k)
    FDA Class 2 ·Radiology

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·May 5, 2014

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·October 15, 2012

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code GZB·August 6, 2010