BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K2-HF BLEACH DENTINE, BD-3, 50g.

    FDA UDI
    Yeti Dentalprodukte GmbH·EYET38621190·

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011862119180·Standard Band, Tooth 45/35, Size 19/Roth 18

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011862119220·Standard Band, Tooth 45/35, Size 19/Roth 22

    UreTron PF Series Probe

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

    HLR MODEL 601 HEART LUNG RESUSCITATOR AND HEARTSAVER 100

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·October 8, 2010

    RETROFLEX 3/ SAPIEN INTRODUCER SHEATH SET

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYB·December 7, 2012

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·June 10, 2014

    OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

    FDA Enforcement
    Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012