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 ×

    GK ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    HDC STERILE SELF LIGATING SPIDER SCREW, MODEL SLI,SL2

    FDA 510(k)
    FDA Class 2 ·Dental

    ANTI-BLASTOMYCES SERUM #CF10027X

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ELECSYS 2010 RACK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·November 4, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·January 31, 2014

    XIA TITANIUM 4.5 POLYAXIAL SCREW DIAM 4.5 X 25

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code KWP·December 21, 2012