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.

    STIMULATOR MODEL 8021

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACCIN UNIPOLAR HEAD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Deformity Analysis and Correction Software (DACS) and Instrumentation

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 3, 2014

    INQUIRY STEERABLE CATH. 6F, 1110-6-25-L

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, IRVINE·Product code DRF·October 5, 2012

    RUSCH GREENSPEC FO HANDLE SMALL

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CCW·May 18, 2015