BEUDAMED
    11 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 ×

    KIRSCHNER NEER-III MODULAR PROXIMAL HUMERUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228746431·GC Initial™ Ti Inside IN-43 Sun, 50g

    DETERMINE HIV-1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·October 10, 2024

    DETERMINE HIV-1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·December 16, 2024

    DETERMINE HIV-1/2 AG/AB COMBO 25T

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code MZF·December 16, 2024

    S.L.T. LASER DELIVERY HANDLES W/SURGICAL RODS

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

    SOLAR

    FDA 510(k)
    FDA Class 1 ·Dental

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 24, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code NKB·December 15, 2012

    TDX/TDXFLX CANNABINOIDS REAGENT

    FDA Adverse Event
    Injury ·ABBOTT HEALTH PRODUCTS, INC.·Product code LDJ·November 8, 2006