BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    MICROSTREAM FILTERLINE ICU

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Stryker iVAS 13g Bone Biopsy Kit

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

    GENERATORS, ATRIAL INHIBITED PULSE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    ARCHITECT C4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 31, 2018

    MAGNUM2 KNOTLESS IMPLANT

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code HTY·February 22, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·February 3, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 5, 2014

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code FMI·September 1, 2009