BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

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    ADVANCED IN-BED WEIGH SYSTEM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ChoICE Guide Wire, Mailman Guide Wire, Luge Guide Wire, ChoICE PT Guide Wire, PT Graphix Wire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUCRALFATE AND CARAFATE PASTE KITS

    FDA 510(k)
    FDA Unclassified ·Unknown

    CURLIN 4000CMS IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code FRN·January 9, 2013

    FIXODENT DENTURE ADHESIVE, VERSION UNKNOWN (CALCIUM ZINC GANTREZ SALT 33 %, CELL

    FDA Adverse Event
    Other ·PROCTER & GAMBLE MFG CO.·Product code KOO·December 13, 2010

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·July 18, 2014

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021