BEUDAMED
    8 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ZEPHYR ENDOBRONCHIAL VALVE SYSTEM

    FDA Adverse Event
    Malfunction ·PULMONX CORP.·Product code NJK·September 22, 2025

    ZEPHYR ENDOBRONCHIAL VALVE

    FDA Adverse Event
    Malfunction ·PULMONX, CORP·Product code NJK·August 6, 2025

    ZEPHYR ENDOBRONCHIAL VALVE

    FDA Adverse Event
    Injury ·PULMONX, CORP.·Product code NJK·April 28, 2025

    ZEPHYR ENDOBRONCHIAL VALVE

    FDA Adverse Event
    Malfunction ·PULMONX CORP.·Product code NJK·May 19, 2025

    ZEPHYR

    FDA Adverse Event
    Injury ·PULMONX, CORP.·Product code NJK·January 12, 2022

    UNKNOWN EMPRINT ANTENNA

    FDA Adverse Event
    Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code NEY·August 18, 2021

    PULMONEX XENON SYSTEM

    FDA Adverse Event
    Injury ·BIODEX MEDICAL SYSTEMS, INC.·Product code IYT·September 22, 1998

    PULMONOX II

    FDA Adverse Event
    Injury ·PULMONOX MEDICAL CORP.·Product code MRP·February 12, 1997