BEUDAMED
    7 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 ×

    OSTEONICS(R) ARC DEPOSITIONED FEMORAL COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Terran NM-101

    FDA 510(k)
    FDA Class 2 ·Radiology

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 22, 2016

    SEVEN CONTINUOUS GLUCOSE MONITORING

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·January 25, 2013

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Death ·REYNOSA MANUFACTURING·Product code FKX·November 9, 2010

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Death ·BAXTER HEATHCARE CORPORATION·Product code FKX·July 11, 2014