BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Pathology

    TE7/TE5/TE7 Max/TE5 Max/TE9 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    High Retention Attachment System

    FDA 510(k)
    FDA Class 2 ·Dental

    BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·November 30, 2017

    X100L BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·April 12, 2017

    X100L BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·April 7, 2017

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·November 11, 2014

    INBONE(TM) STEM TIBIAL MID

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HSN·September 12, 2011

    GALILEO NEO

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·July 23, 2013

    BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·April 4, 2018

    BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·March 15, 2018

    BD ULTRASAFE PASSIVE¿ X-SERIES NEEDLE GUARD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON HUNGARY KFT (BD)·Product code MEG·March 15, 2018