BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING

    FDA 510(k)
    FDA Not Classified ·Unknown

    VARIAX

    FDA UDI
    Stryker GmbH·07613327302615·Compression plate trials insert

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867524132·ECLIPSE SIZING PLATE, 49

    LONG PULSE ND: YAG LASER SYSTEM

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

    SKINTACT ECG ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FRN·April 7, 2014

    3.5MM 90-S SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·December 9, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·February 2, 2013