BEUDAMED
    6 results · 25ms · 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.

    RESPIRONICS BAGEASY ENCOR ADULT SEMI-REUSABLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    URESIL FIXATION DEVICE

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

    COMPAC(TM) DIODE LASERS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 4, 2013

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MQM·December 21, 2010

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 15, 2014