BEUDAMED
    6 results · 20ms · 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 ×

    ORTHODONTIC ARCH WIRE

    FDA 510(k)
    FDA Class 1 ·Dental

    TC-1000, TC-1050 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TENTATIVE OPERATING NAME-JAZZ BAND

    FDA 510(k)
    FDA Class 2 ·Dental

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 22, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·December 7, 2010