BEUDAMED
    9 results · 29ms · 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 ×

    CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994435705·SCREW 7892530 HA COATED NONCAN 5.5 X 30

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756277891·PIN REMOVAL KIT

    Surefil one Self-adhesive Composite Hybrid

    FDA 510(k)
    FDA Class 2 ·Dental

    SPRYTIE, MODELS ST001, ST002 AND ST003

    FDA 510(k)
    FDA Class 2 ·Dental

    VNGD SSK PSC TIB BRG 18X71/75

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 23, 2016

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 24, 2014

    SABO SAG SAW

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·November 2, 2010

    19 CM 14.5 FR HEMOSTAR STANDARD KIT

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code MSD·December 26, 2012