BEUDAMED
    6 results · 18ms · 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.

    RING-ORIFICE, TURBULENT FLOW PNEUMOT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    RIA, CORTISOL KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 21, 2014

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    BIOSURE INSTRUMENTS

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code NBH·May 22, 2015