BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO CARDIAC STATUS CK-MB/MYOGLOBIN RAPID ONE-STEP TEST, LIFESIGN MI CK-MB/MYOGLOBIN, LIFESIGN CK-MB/MYOGLOBI

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Silhouette Featherlift / Silhouette Lift

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

    SPECTRANETICS TURBO-TANDEM SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERRAD 100S STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 8, 2006

    ZEPHIR ANTERIOR CERVICAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009

    PWRD ECH FLEX 60MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 6, 2013

    VIRTUOSO DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    CAPSUREFIX

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code NVN·August 8, 2014

    STERRAD 100NX STERILIZER 1-DR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 6, 2021