BEUDAMED
    7 results · 21ms · 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 ×

    TRIMETHOPRIM/SULPHAMETHOXAZOLE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983027·posteriors; shade A3.5; size L; lower jaw

    Steerable catheter control system

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PATIENT EXAM GLOVES (MFG JET FAR INDU. INC.)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    2520274-2013-10658

    FDA Adverse Event
    Malfunction ·Product code MNI·February 26, 2013

    ENTERRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LNQ·February 4, 2011

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·August 6, 2014