BEUDAMED
    6 results · 26ms · 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.

    SUTURE KITS STERILIZED W/GAMA RADIATION

    FDA 510(k)
    FDA Unclassified ·Unknown

    EXTERNAL SILASTIC BOOT FOR CARDIAC PULSE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Thermo Scientific Oxoid Rezafungin Disc (5 µg) RZF5

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 27, 2014

    PROLENE POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 14, 2012

    COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 13, 2010