BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    GC CULTURE MEDIUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    IV SET AN120 W/O BP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·April 26, 2019

    Altus Spine Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTUITIVE SURGICAL ULTRASONIC SHEARS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·March 31, 2025

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·May 15, 2014

    3M RED DOT MONITORING ELECTRODE

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE·Product code DRX·August 11, 2010