BEUDAMED
    7 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.

    MULTIPACE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CRI CYNOSAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WHEELCHARIOT LIGHTWEIGHT MANUAL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SHELL POROUS WITH CLUSTER HOLES

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·May 26, 2017

    HUDSON POCKET PEAK, PEAK FLOW METER

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code CAF·January 23, 2013

    VITROS ECI IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·December 21, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 4, 2014