BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Lubricating Jelly

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MULLINS-X PTV CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COBE ANGEL WHOLE BLOOD SEPARATION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 30, 2018

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 30, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 6, 2014

    LIFECOICE

    FDA Adverse Event
    Injury ·INOVA LABS·Product code CAW·March 30, 2013

    INTELLIVUE INFORMATION CENTER CLIENT

    FDA Adverse Event
    Death ·PHILIPS HEALTHCARE - ANDOVER·Product code MHX·June 21, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·November 12, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 5, 2021