BEUDAMED
    6 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.

    IMACK-MB, CATALOGS 602-1, 602-1/125, 602-1/225

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Double Flexible Tipped Wire Guides

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO JOURNEY UNICONDYLAR FEMORAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·June 18, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 18, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 17, 2012