BEUDAMED
    7 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 ×

    QBC ACCUTUBE(423406)/QBC AUTOREAD(424571)

    FDA 510(k)
    FDA Class 2 ·Hematology

    CODE MASTER XL

    FDA Adverse Event
    Malfunction ·HEWLETT-PACKARD COMPANY·Product code LDD·September 6, 1996

    MYLAB30, 50, 70 AND 90 SYSTEMS ADDITION OF 3D/4D, MODELS 7300, 7350, 6150, 6100

    FDA 510(k)
    FDA Class 2 ·Radiology

    Pantheris Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·June 27, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·February 14, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·December 17, 2010