BEUDAMED
    8 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 ×

    DECAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993147·anteriors; shade A4; mould IS

    CHEM-CHEX-ALT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Stereotaxis Genesis RMN with Navigant Workstation (NWS) and Cardiodrive System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INSERT, BIPOLAR FORCEPS

    FDA Adverse Event
    Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code GEI·April 2, 2015

    ARCHITECT CA 19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code NIG·March 7, 2013

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 7, 2011

    SPRINT FIDELIS

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