BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HOWMEDICA FEMORAL & PROXIMAL TIBIAL MODULAR REPLACEMENT SYTESM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIMPLICI-T ANNULOPLASTY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Dynarex Xeroform Petrolatum Dressing

    FDA 510(k)
    FDA Unclassified ·Unknown

    MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 26, 2021

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLM·May 20, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LWP·February 9, 2013

    5MM NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 7, 2011