BEUDAMED
    6 results · 25ms · 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.

    DERMIVIEW HYPOALLERGENIC CLEAR TAPE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DENSICOMP 250

    FDA 510(k)
    FDA Class 2 ·Radiology

    AVL MODEL 982 ELECTROLYTE ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·February 5, 2013

    WIRELESS FOOTSWITCH

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code JAA·December 19, 2010

    AMS SPECTRA CONCEALABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS (MN)·Product code FAE·July 18, 2014