BEUDAMED
    8 results · 22ms · 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 ×

    LEADPOINT FOCUS WORKSTSTION, LEADPOINT FOCUS NOTEBOOK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Biogel

    FDA UDI
    Bosma Enterprises·10818634023855·Biogel Skinsense Indicator Underglove Surgical ...

    CONTOUR HA COATED RECONSTRUCTION RING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENSPIRE DISCECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    23 G X .75 IN. BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 8, 2017

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·May 31, 2013

    MX-PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·June 15, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·September 3, 2008