BEUDAMED
    19 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    CADD-LEGACY 1 AMBULATORY INFUSION SYSTEM MODEL NUMBER 6400

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CADD LEGACY PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·April 11, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 8, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 23, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 22, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 22, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 8, 2022

    CADD LEGACY PLUS PUMPS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·October 29, 2022

    CADD LEGACY PLUS PUMPS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·October 24, 2022

    Brigade

    FDA UDI
    Nuvasive, Inc.·00887517967299·Brigade Lateral, 8x38x28mm 15°

    7982838

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 15, 2023

    ORLUS MINI SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    Geistlich Derma-Gide

    FDA 510(k)
    FDA Unclassified ·Unknown

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·January 20, 2025

    CADD-LEGACY® PCA AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD INC.,·Product code MEA·March 29, 2016

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 9, 2022

    HEARTSTART XL+DEFIB/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 13, 2014

    SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code JDN·February 28, 2013

    CE INFUSOR LV 5, 12 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 9, 2011