BEUDAMED
    7 results · 28ms · 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 ×

    Merit Siege Vascular Plug

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICROEEG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    EON MINI

    FDA Adverse Event
    Injury ·ST JUDE MED - NEUROMODULATION·Product code GZB·October 24, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 16, 2011

    LIGACLIP MCA SMALL

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDO·July 9, 2013

    DRX Revolution Mobile X-Ray System

    FDA Enforcement
    Class II ·Ongoing·Carestream Health, Inc.·December 13, 2023