Magnetic Resonance Imaging (MRI) Information for Cordis Devices

Cordis provides detailed MRI safety and compatibility information to support healthcare professionals in making informed decisions when imaging patients with Cordis devices. The following MRI Letters contain device-specific conditions, classifications (e.g., MR Safe, MR Conditional), and technical parameters relevant for performing MRI procedures safely.

Each document is intended for use by clinicians and radiology professionals who require technical MRI guidance for Cordis implantable and interventional products. The following products are no longer commercially available: VELOCITY Stent, SONIC Stent, PALMAZ SCHATZ Stent, CROSSFLEX Stent and CYPHER Stent.

Please review the letters below for product-specific MRI guidelines. If additional information is needed, contact the Cordis Medical Information Center.