BEUDAMED
    9 results · 19ms · 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 ×

    HEMODIALYSIS CONCENTRATE ADDITIVES

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

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209104215·KIT, EAGLE IFAK - BLEEDER - MTC

    Fix-it Polymer

    FDA UDI
    JBC and Company·D851431·Quick Set Clear Powder

    FIX-C PEEK ACIF SA System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PAN-AM MYELOGRAM TRAY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HOMECHOICE PRO

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

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FPA·November 29, 2012

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code MGB·September 29, 2010

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021