BEUDAMED
    8 results · 20ms · 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 ×

    TIMESH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIEMENS SONOLINE SI-450, OB/GYN,ENT,DENTAL DEVICES

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFIED RETINAL CAMERA MODEL CR4-45NM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159211·

    ZMR®

    FDA UDI
    Zimmer, Inc.·00889024159228·

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014