BEUDAMED
    8 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.

    CP BODY ARRAY/ CP SPINE ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515243453·Ostrum Antrum Punch, rt

    SURGICAL INSTRUMENT MANUFACTURERS, LLC

    FDA registration
    SURGICAL INSTRUMENT MANUFACTURERS, LLC·87 products·🇺🇸 United States

    NASCOR OXYDOME

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PACEVIEW

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·January 30, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·December 22, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 15, 2014