BEUDAMED
    8 results · 28ms · 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 ×

    SAFESITE INJECTION SITE AND BLUNT CANNULA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SmartLinx Vitals Plus Patient Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FIXATION TROCARS

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

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 8, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 8, 2024

    FLEXI-SEAL SIGNAL FECAL MANAGEMENT SYSTEM KIT

    FDA Adverse Event
    Injury ·CONVATEC INC·Product code KNT·June 9, 2014

    SYNCHRON® LX20 PRO CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·October 26, 2010

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 21, 2012