BEUDAMED
    8 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 ×

    STREP ID TRIPLATE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DD cubeY® HL

    FDA UDI
    Dental Direkt GmbH·EDDIG8440191·The DD cubeY® HL zirconium dioxide milling blan...

    BIGGY AGAR NICKERSON MEDIUM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    K-TUBE REPAIR KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    8CH INFINITY DBS LEAD KIT, 40CM, 1.5, B

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MHY·July 31, 2023

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 2, 2014

    4.5MM/3.5MM TI LCP® METAPHYSEAL PLATE 16 HOLES

    FDA Adverse Event
    Injury ·SYNTHES·Product code LXT·November 24, 2012

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·September 13, 2010