BEUDAMED
    13 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.
    Filters Regulation: Us FDA ×

    MODIFIED BLOOD RECIPIENT SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169205956·CONNECTOR 5993120 4.75-4.75 CLSD LAT 20S

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993120·anteriors; shade A3.5; mould UCS

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198123·AK3 PS Insert Trial Size 1, 20mm

    Galaxy Fixation System

    FDA UDI
    ORTHOFIX SRL·18054242511526·MEDIUM MULTISCREW CLAMP STERILE

    Real Intelligence Cori

    FDA 510(k)
    FDA Class 2 ·Neurology

    XENIUM XPM 110, XENIUM XPM 130, MODELS M25649A, M25650A, XENIUM XPM 150, XENIUM XPM 170

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

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 4, 2018

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 31, 2018

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 3, 2018

    HI -TORQUE BALANCE MIDDLEWEIGHT GUIDEWIRE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code DQX·February 26, 2013

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·August 8, 2014

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 8, 2011