BEUDAMED
    6 results · 21ms · 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.

    TEFLON FEMORAL CATHETER MWI 100,10 &

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

    NATURALASE LP ND:YAG LASER

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

    POWDER FREE VINYL PATIENT EXAMINATION GLVOES, LIGHT YELLOW COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PFC SIGMARP STB TB IN 4 12.5

    FDA Adverse Event
    Injury ·DEPUY (IRELAND) 9616671·Product code NJL·May 27, 2014

    ASR ACETABULAR IMPLANT 48

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 14, 2012

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES CLONMEL·Product code NIQ·September 8, 2010