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 ×

    SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DIAMONDBACK 360 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GEODESIC EEG SYSTEM SERIES 100

    FDA 510(k)
    FDA Class 2 ·Neurology

    RENASYS GO NPWT DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW WOUND MANAGEMENT·Product code BTA·November 15, 2012

    PRONTOSAN WOUND-GEL BOTTLE "NORD" 30ML

    FDA Adverse Event
    Injury ·B. BRAUN MEDICAL AG·Product code FRO·May 19, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·September 8, 2010