BEUDAMED
    6 results · 17ms · 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.

    SUCTION TUBES: HOUSE, BARON

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OXIPROBE, MODELS BM-100, BM-200, BM-400, BM-300, BM-300S, BM-600P

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Byteflies Kit

    FDA 510(k)
    FDA Class 2 ·Neurology

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 24, 2014

    ALARIS SE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·November 3, 2010

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·December 20, 2012