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 ×

    AVI MODEL 2012, 1.2 MICRON FILTER IV ADMINISTRA.

    FDA 510(k)
    FDA Class 2 ·General Hospital

    THOMPSON TYPE RASP W/TOMMY BAR

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    VITRECTOMY PACK #J120

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 22, 2014

    PAD CONNECTOR CABLE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 20, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021