BEUDAMED
    7 results · 25ms · 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.

    MARKLEY THREADED WIRE

    FDA 510(k)
    FDA Class 1 ·Dental

    TEMPUS PRO PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endoscopy Irrigation Tubing

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LOGIC TIBIA PS MOD INSRT SZ 3 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 24, 2024

    THERAKOS CELLEX SYSTEM

    FDA Adverse Event
    Malfunction ·THERAKOS INC.·Product code LNR·May 9, 2014

    SMALL CLIP APPLIER

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 13, 2012

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010