BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    RED DOT CARDIAC SENSOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IRON REAGENT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MDP DISPOSABLE SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 13, 2014

    TENDRIL DX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    REJUVENATE MODULAR NECK

    FDA Adverse Event
    Injury ·STRYKER IRELAND, LTD. OSTEONICS (ORTHOPAEDICS DIVI·Product code JDI·December 27, 2012

    EV3 Pipeline Flex Embolization Device with Flex Shield Technology

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021