Bilio-Pancreatic Strictures

1. Meining A. et al. Direct Visualization of Indeterminate Pancreaticobiliary Strictures using Probe-based Confocal Laser Endomicroscopy – A Multicenter Experience. 
Gastrointestinal Endoscopy, 2011.
2. Meining A. et al. Classification of Probe-based Confocal Laser Endomicroscopy findings in Pancreaticobiliary Strictures. Endoscopy, 2012.
3. Caillol F, Bories E, Autret A, Poizat F, Pesenti C, Ewald J, Turrini O, Delpero JR, Monges G, Giovannini M. Evaluation of pCLE in the bile duct: final results of EMID study : pCLE: impact in the management of bile duct strictures. Surg Endosc. 2014 Dec 10.
4. Slivka et al. Validation of the diagnostic accuracy of probe-based confocal laser endomicroscopy (pCLE) for the characterization of indeterminate biliary strictures: results of a prospective multicenter. GIE, 2015
5. Caillol et al. Refined Probe-Based Confocal Laser Endomicroscopy Classification for Biliary Strictures: The Paris Classification. Dig Dis Sciences 2013

Cellvizio^® I.V.E. with Confocal Miniprobes^TM are regulated Medical Device, CE marked (CE 0459) (Class IIa – NB : G-MED) and FDA cleared. Cellvizio^® is a registered trademark and Confocal Miniprobe^TM is a trademark of Mauna Kea Technologies. The Cellvizio^® I.V.E. is a confocal laser system with fiber optic probes that are intended to allow imaging of the internal microstructure of tissues including, but not limited to, the identification of cells and vessels and their organization or architecture. Once connected to the Cellvizio^® I.V.E.: the CholangioFlex^TM N Confocal Miniprobes^TM are intended to allow imaging of the upper gastrointestinal tract including biliary and pancreatic ducts accessed by an endoscope or endoscopic accessories. Please consult labels and instructions for use. These statements and the associated reference to specific clinical studies, are not intended to represent claims of safety or effectiveness for detecting or treating any specific condition or disease state. Rather this information is intended to provide useful reference to selected published literature describing physician experiences with the associated clinical uses. Any diagnostic assessment should always be made by the attending physician, based on the evaluation of all sources of clinical, endoscopic and other relevant information. These statements have not been reviewed, cleared, or approved by the U.S. FDA. The use of this medical device is exclusively reserved for health professionals. Product availability cannot be guaranteed in all countries. For further information, please contact your local sales representative.