BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    MONOJECT STERILE M200 ALUMINUM/M250 POLYPROPYLENE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209135745·

    ANGIOSCOPY CATHETER

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

    TRYPTIC SOY BROTH W/6.5%SODIUM CHLORIDE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 6, 2014

    MAMMOMARK BIOPSY IDENTIFIER

    FDA Adverse Event
    Malfunction ·DEVICOR MEDICAL PRODUCTS INC.·Product code NEU·November 29, 2012

    ASR UNI FEMORAL IMPL SIZE 41

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·September 29, 2010