BEUDAMED
    6 results · 18ms · 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 ×

    PULSE*SPRAY INJECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LUMINEX LL LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Multi Modality Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    STELLARIS 25G VITRECTOMY PACK W AFI&WF

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·May 30, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 20, 2010

    ASPHERE M SPEC 12/14 36 +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 15, 2013