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 ×

    HOWMEDICA MAINSTAY ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REDDICK RETRACTOR

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PTI ANNULOPLASTY RING(STERILE)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

    CANES

    FDA Adverse Event
    PINGHU WEIFENG MATERIAL TECHNOLOGY·Product code IPS·July 29, 2014