BEUDAMED
    6 results · 18ms · 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 ×

    ARTHROSCOPE OPERATIVE KNIFE SET

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    SOFTXIL

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    HDC STERILE SPIDER SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·April 24, 2014

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Death ·ZOLL MEDICAL CORP·Product code MKJ·September 27, 2012

    ONE STEP COMPLETE ELECTRODE

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MLN·July 21, 2010