BEUDAMED
    7 results · 20ms · 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 ×

    Compression Therapy Device Model LGT-2200SP

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    VIEWRAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    NESSI SPACER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    QUARTET

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 26, 2013

    CS300

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·July 29, 2011

    BD POSIFLUSH NORMAL SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·September 30, 2020