Bracco Diagnostics Inc. has announced that the U.S. Food and Drug Administration (FDA) granted import discretion of Iomeron (iomeprol injection) into the U.S. to address the ongoing iodinated contrast media shortage. The product addresses the need for the most advanced diagnostic imaging standards and will be temporarily available in the U.S. market starting at the end of August, 2022.
Whale Imaging Launches New G-Arm Duo Imaging System
Bracco Announces FDA Approval of Gadopiclenol Injection, a New Macrocyclic High-Relaxivity Gadolinium-Based Contrast Agent which will be commercialized as VUEWAY™ (gadopiclenol) injection and VUEWAY™ (gadopiclenol) Pharmacy Bulk Package by Bracco
Contrast Media Imaging Technology News
Kodak Receives FDA Clearance for New DR System
Simplifying Computed Tomography Angiography (CTA)
S-1
Surgical C-Arm Combines Advantages of Other Tables
FDA Approves New MRI Contrast Agent for Nervous System Imaging
Imaging Technology News
PDF) Use of Intravenous Gadolinium-Based Contrast Media in Patients With Kidney Disease: Consensus Statements from the American College of Radiology and the National Kidney Foundation