BEUDAMED
    8 results · 17ms · 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.

    SLIDEX STAPH-KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AG GARMENTS CONDUCTIVE ELECTRODES, MODELS 100-104 SLEEVES,110-114 GLOVES,120-124 SOCKS,130-132 PANELS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ETHICON ENDO-SURGERY ENSEAL G2 CORDLESS TISSUE SEALERS

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

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·June 16, 2009

    NEXGEN LEGACY PROVISIONAL/CUTTING GUIDE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LXH·November 9, 2010

    VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KHO·January 18, 2013

    QUICKFLEX XL LV LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·July 9, 2014

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·August 8, 2025