BEUDAMED
    7 results · 20ms · 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 ×

    KSEA DISPOSABLE TUBING SET FOR THE ARTHROPUMP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WINDSURFER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NET Brand Small Fragment and Large Fragment Osteosynthesis Plating System, NET Brand of DHS/DCS Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN EXTERNAL NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·August 6, 2013

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 8, 2013

    FIXATION KIT FOR E5280 AND E5260 SENSORS

    FDA Adverse Event
    Injury ·RADIOMETER MEDICAL APS·Product code DQA·October 19, 2010

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE INC.·Product code LZG·July 11, 2014