BEUDAMED
    9 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 ×

    PERFECTA REVISION HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LITHOTRIPTOR SYSTEM MODEL 27080

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

    USCI(R) HEMAFLEX(TM) INTRODUCER WITH COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 16, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 11, 2013

    TECNIS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·July 24, 2014

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    ALP 501

    FDA Adverse Event
    Injury ·CURRIE MEDICAL SPECIALTIES·Product code JOW·September 1, 2012

    ALP 501

    FDA Adverse Event
    Injury ·CURRIE MEDICAL SPECIALTIES·Product code JOW·July 25, 2012