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.

    STERILE EQUIPMENT COVERS

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

    ILT SAFE CROSS 0.035 SUPPORT CATHETER, MODEL C135SN1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FACET FIXX

    FDA 510(k)
    FDA Unclassified ·Unknown

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 26, 2014

    PNEUPAC PARAPAC

    FDA Adverse Event
    Injury ·SMITHS MEDICAL INTERNATIONAL LTD.·Product code BTL·January 3, 2013

    C-TEK IMPLANTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·December 17, 2010