BEUDAMED
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    RADIOLUCENT ECG ELECTRODE MODEL NO: 1680

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medline-Microtek

    FDA UDI
    Microtek Medical LLC·00748426144921·Patient Drape, Patient Isolation Drape, 244 cm ...

    UA-CELLULAR FOR IQ

    FDA 510(k)
    FDA Class 2 ·Hematology

    CORUS Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PYRAMESH® IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code EZX·July 17, 2014

    GIALLOY CB/N

    FDA UDI
    SRL Dental GmbH·ESRL58902011·Aufbrennfähige Nichtedelmetall-Dental-Gusslegie...

    ANEURX ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code MIH·October 22, 2010

    RIATA PASSIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012

    ARTICULEZE M 28MM 1.5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code JDI·June 24, 2014

    PYRAMESH IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code EZX·December 9, 2016