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 ×

    REPEL(TM) LITE CUT RESISTANT GLOVE LINERS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    POWDER FREE (BLUE) NITRILE PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Digital Thermometer, Model: DT007, DT008

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·January 14, 2013

    SITTER SELECT

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·November 19, 2010

    SECUR-FIT HA 132 HIP STEM #10

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·July 3, 2014

    Pipeline Flex Embolization Device

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