BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    ASCENT KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Monolith

    FDA UDI
    Nuvasive, Inc.·00887517697981·Monolith Core, Ø14x28mm

    NONE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code UNK·December 11, 2009

    ECG Cable

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EASYONE PRO RESPIRATORY ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TENOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·December 11, 2009

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 6, 2013

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    CAPSURE EPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·February 15, 2011