BEUDAMED
    37 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    REBOA Balloon Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PENRITH ELETTRA ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    SMR REVERSE SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD BACTEC¿ MGIT¿ 960 PZA KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·April 25, 2023

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code MJA·February 2, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code MJA·January 30, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSO & CO.·Product code MJA·January 30, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code MJA·February 2, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code MJA·February 2, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code MJA·January 30, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code MJA·February 2, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code MJA·February 2, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code MJA·February 2, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code MJA·January 30, 2024

    BD MGIT 960 PZA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code MJA·February 2, 2024

    BD BACTEC¿ MGIT¿ 960 PZA KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·April 25, 2023

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code ILS·June 10, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 6, 2011

    INDY OTW VASCULAR RETRIEVER

    FDA Adverse Event
    Injury ·COOK INC·Product code MMX·December 23, 2016