BEUDAMED
    8 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 ×

    Omnimax S3, Omnimax S4

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517570512·CoRoent Ant TLIF Ti, 13x13x30mm 4°

    RXG DISTRACTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO DASH 3000/4000 PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYRINGE 0.5ML 31GA 8MM UFII 10BAG 500CS

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE - HOLDREGE, NE / 68949·Product code FMF·February 12, 2024

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·September 2, 2011

    SYMBIQ

    FDA Adverse Event
    Malfunction ·HOSPIRA GLOBAL MEDICAL AFFAIRS, DIRECTOR GLOBAL COMPLAINT MANAGER·Product code FRN·November 10, 2008

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 18, 2013