BEUDAMED
    27 results · 25ms · Sources: EU EUDAMED, US FDA

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    SeaSpine Navigation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·July 25, 2024

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·July 25, 2024

    BD NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·December 2, 2025

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·December 16, 2024

    BD NEEDLE FILTER

    FDA Adverse Event
    Injury ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·December 24, 2025

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·September 23, 2024

    ILAB ULTRASOUND IMAGING SYSTEM, VERSION 1.3

    FDA 510(k)
    FDA Class 2 ·Radiology

    TIGER 500 SERIES HIGH SPEED HANDPIECES AND ATTACHMENTS

    FDA 510(k)
    FDA Class 1 ·Dental

    BD NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Injury ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·December 18, 2025

    BD NOKOR¿ FILTER AND ADMIX NEEDLES

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·October 3, 2023

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·March 27, 2025

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·July 16, 2025

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·May 26, 2025

    NEEDLE FILTER 19X1-1/2 TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code GAA·July 16, 2025

    UNKNOWN INJECTION NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·March 19, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 17, 2013

    ACCU-CHEK ACTIVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 19, 2008

    ACCESS 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 24, 2011

    NOT APPLICABLE

    FDA Adverse Event
    Injury ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·December 31, 2025