BEUDAMED
    7 results · 19ms · 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 ×

    ADMIRA

    FDA 510(k)
    FDA Class 2 ·Dental

    HOTDOG MULTI FUNCTION CONTROLLER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POSITRON EMISSION COMPUTED TOMOGRAPH SET-1400W

    FDA 510(k)
    FDA Class 2 ·Radiology

    NOVASURE

    FDA Adverse Event
    Malfunction ·HOLOGIC, INC·Product code MNB·March 1, 2013

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    BUTTON REPLACEMENT GASTROSTOMY DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·February 16, 2011

    STERRAD® NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 20, 2018