OptiStar™ Elite Contrast Delivery System is a medical device intended for use by qualified healthcare professionals. It is intended to inject MR contrast media and flushing solutions into a patient's vascular system to obtain diagnostic images when used in conjunction with Magnetic Resonance (MR) Imaging equipment. Class IIb/CE TÜV SÜD 0123 Manufacturer: Liebel-Flarsheim Company LLC EC Rep: Guerbet.
Contrast& Care® is a medical device intended for use by healthcare professionals only. It allows imaging centers to collect, archive, view and share patients' injection data, including data concerning contrast products, adverse events, injector activity, data on the estimated eGFR and other pre-exam alerts, such as previously reported allergies. Contrast&Care® also provides options to review protocols, create protocol libraries, and visualize analytics data and trends relating to injection activity and contrast product usage. Class I/CE Manufacturer: Medex.
Contrast& Care®+ is a medical device for use by healthcare professionals only. It enables imaging centers to collect, archive, review, and share patient injection data. This data can include contrast media details, associated disposables, adverse events, injector activity, history of previous contrast media administration, eGFR information, and other pre-exam alerts, such as previously reported allergies. It also provides features to review protocols, create protocol libraries, send injection protocols to compatible injectors, visualize analytics and trends related to injection activity and contrast media usage. Class I/CE Manufacturer: Medex.
For use only in countries with applicable health authority registrations.
For complete information about precautions and optimal usage conditions, we recommend consulting the instruction for use supplied with these devices or by your local Guerbet representative(s).
OptiStar™, Contrast& Care®, OptiProtect™, Timing Bolus® , Patency Check® are trademarks of Guerbet.
© Guerbet Group 2022. P22001712 - December 2022
*Data on file; D12582 A; D12766 Rev A; D11839 Rev A. Next generation GBCA from Guerbet being under evaluation by European Health Authorities (EMA) and for use only in countries with applicable health authority registrations. FDA approved.
GBCA = Gadolinium-Based Contrast Agents