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

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    E-CUBE 15

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCENARIA WHOLE-BODY X-RAY CT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MASIMO LNOP/LNCS/M-LNCS MULTISITE-L OXIMETRY SENSORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    V12 COVERED STENT

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code JCT·May 15, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 9, 2011

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·August 13, 2008

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 25, 2017

    COREVALVE REVALVING SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 25, 2017