BEUDAMED
    7 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 ×

    INTERTECH STERILE WATER FOR INHALATION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OIC Intramedullary Nail System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GORE VIABIL BILILARY ENDOPROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TERUMO STERNAL SAW II

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GFA·October 1, 2010

    ENGUARD PFX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code DTB·January 13, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 16, 2012

    NV GXL LINER LIPPED 40MM ID, GROUP 4 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·November 15, 2023