BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209107353·KIT, BLEEDING CONTROL - #1

    Retraction Aspirator

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CERAM X UNIVERSAL MANO-CERAMIC RESTORATIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    QUIK-COMBO PACING/DEFIBRILLATION/ECG

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORP·Product code LDD·March 31, 1998

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 5, 2014

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD·Product code GCX·November 14, 2012

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·September 28, 2010