BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    TRACHEA/CUFF INFLATOR W/PRESSURE #583

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LINICAL PROTEIN 2 CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER ARRAY PROTEIN SYSTEMS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MOBILETT Impact

    FDA 510(k)
    FDA Class 2 ·Radiology

    FLOEY CATHETER W TEMP

    FDA Adverse Event
    Injury ·DEGANIA SILICONE LTD·Product code DRF·October 17, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code KOD·July 7, 2017

    AU480 CLINICAL CHEMISTRY ANALYZER WITH ISE

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JGS·May 25, 2014

    FORCEPS MCL19 LEFT BOUCHAYER HEART [MXI/XOM]

    FDA Adverse Event
    XOMED MICROFRANCE MFG·Product code LRC·November 14, 2012

    EPIC II VR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2010

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV (USD)·Product code DRF·November 9, 2018