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 ×

    Nexxis OR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ponto

    FDA UDI
    Oticon Medical AB·05712149013968·Ponto Soft band, navy

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 17, 2022

    PLEXUS EBV IGM MULTI-ANALYTE DIAGNOSTICS, MODEL: MP0600M

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MYSONO U6 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    GYNECARE TVT SECUR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code PAH·June 17, 2013

    FLEX CUP

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC·Product code HDB·September 28, 2014

    SPEEDBAND SUPERVIEW SUPER 7, MODELS 4205

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·July 23, 2011