BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    SAGITTAL KNEE TESTER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    EasyTouch

    FDA UDI
    MHC MEDICAL PRODUCTS, LLC·MHC18310412·

    Easter S.L Bracket, .022 Roth, LR1

    FDA UDI
    Astar Orthodontics Inc.·06941673516174·

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·FEEL TECH BIO CO., LTD.·Product code FMI·June 20, 2023

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·MHC MEDICAL PRODUCTS, LLC·Product code FMI·April 26, 2023

    FLUENCY TRACHEOBRONCHIAL STENT GRAFT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ADVANCED PERFUSION SYSTEM 1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMI·June 20, 2023

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·May 23, 2014

    REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 8

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·November 2, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 7, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018