BEUDAMED
    7 results · 19ms · 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.

    ElectroTek

    FDA 510(k)
    FDA Class 2 ·Neurology

    METASURG SUBTALAR IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XINIWAVE, MODEL XW-18

    FDA 510(k)
    FDA Class 2 ·Neurology

    RESTYLANE, RESTYLANE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·June 11, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·July 21, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 14, 2014

    TASUKI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·June 6, 2019