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

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    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code OWB·November 30, 2020

    Model 6000 CMS, CMS IOD, or Plus Ambulatory Infusion Pump, Model Number: 360-1101

    FDA Recall
    Terminated ·Curlin Medical Llc·Product code FRN·May 30, 2008

    Physio-Control LIFEPAK 20 defibrillator/monitor is indicated for the termination of certain potentially fatal arrhythmias, such as ventricular fibrillation and symptomatic ventricular tachycardia.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code LDD·April 16, 2008

    Medtronic COMPLETE SE Self Expanding Biliary Stent System, Model number SC760L, includes a pre-loaded self-expanding Nickel-Titanium (Nitinol) stent with 8 tantalum radiopaque markers, 4 on each end, and an over the wire retractable sheath delivery system.

    FDA Recall
    Terminated ·Medtronic Cardiovascular·Product code FGE·November 24, 2008

    GE Healthcare, CT Perfusion 4 on Advantage Workstation, CT and PET/CT consoles. Image analysis software package that allows the user to produce image data and to generate information with regard to changes in image intensity over time supporting CT Perfusion images.

    FDA Recall
    Terminated ·GE Medical Systems, LLC·Product code JAK·May 4, 2009

    iPico Product Usage: Muscle stimulation

    FDA Recall
    Terminated ·Ion Genius, Inc.·Product code NFO·January 6, 2012

    Perfector Product Usage: Muscle stimulation

    FDA Recall
    Terminated ·Ion Genius, Inc.·Product code IPF·January 6, 2012

    Ion Magnum Product Usage: Muscle stimulation

    FDA Recall
    Terminated ·Ion Genius, Inc.·Product code IPF·January 6, 2012

    IELLIOS Product Usage: Muscle stimulation

    FDA Recall
    Terminated ·Ion Genius, Inc.·Product code NFO·January 6, 2012

    Arasys Product Usage: Muscle stimulation

    FDA Recall
    Terminated ·Ion Genius, Inc.·Product code IPF·January 6, 2012

    Portex 3 Way Stopcock Catalog Number: T1103

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code FMG·September 9, 2004

    Portex 3 Way Stopcock Catalog Number: T1202

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code FMG·September 9, 2004

    Portex ULTRA-FLO 4 - Way Stopcock Catalog Number: T1209

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code FMG·September 9, 2004

    Portex Custom Pro-Vent Arterial Blood Sampling Kit Catalog Number: G1481

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JKA·September 9, 2004

    Portex 4-Way Stopcock Catalog Number: T1206

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code FMG·September 9, 2004

    Portex Custom Pro-Vent Arterial Blood Sampling Kit Catalog Number: G1554

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code JKA·September 9, 2004

    Portex 4 Way ''T-Handle'' Stopcock Catalog Number: T1204

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code FMG·September 9, 2004

    Portex High Pressure 4 - Way Stopcock Catalog Number: T8202

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·Product code FMG·September 9, 2004

    Salivary Estradiol ELISA, REF SLV-4188 in vitro diagnostic quantitative measurement of active free Estradiol, an estrogenic steroid, in saliva.

    FDA Recall
    Terminated ·DRG Instruments GmbH Frauenbergstr. 18 Marburg Germany·Product code PEJ·July 14, 2016

    Fiberoptic Bronchoscope Dual-Axis Swivel Adapter Catalog Number: 625191

    FDA Recall
    Terminated ·Smiths Medical ASD, Inc.·September 9, 2004