BEUDAMED
    6 results · 26ms · 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.

    AVTECH LWP*(LOW POROSITY) MWP*(MEDIUM POROSITY)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arthrex Glenoid Intelligent Reusable Instrument System, Arthrex OrthoVis Preoperative Plan, SmartBase for Arthrex Glenoid IRIS, ArthrexVIP Web Portal

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIS HERNIA REPAIR DEVICE, SURGISIS GOLD HERNIA REPAIR GRAFT

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

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 8, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 23, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 10, 2012