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.
    Filters Regulation: Us FDA ×

    POROUS APF/COLLARLESS MODULAR FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    1.5T 12 CHANNEL BODY ARRAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    Stroke VCAR

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    SYBRONPRO XRT

    FDA Adverse Event
    Injury ·EBI INC.·Product code DZE·October 4, 2010

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·November 26, 2012