BEUDAMED
    6 results · 22ms · 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 ×

    PLATELET AGGREGATION REAGENT

    FDA 510(k)
    FDA Class 2 ·Hematology

    NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SOMNOMED MAS RXA

    FDA 510(k)
    FDA Class 2 ·Dental

    M2A-MAGNUM MOD HD SZ 52MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 5, 2014

    ORTHOMET(R) COBALT CHROME FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDI·October 1, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 27, 2012