BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    ANGIOLAZ VES-1CAM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    POST EXTRA SYSTOLIC POTENTIATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMARTRELEASE Endoscopic Soft Tissue Release System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·February 27, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 8, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·August 5, 2014

    SDDRIVE SCREWDRIVER SHAFT T8 105MM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·June 6, 2022