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Higher Gradient Whole-Body MRI Scanner Gets FDA Nod
At an amplitude of 200 mT/m and a slew rate of 200 T/m/s, the gradients for the FDA-cleared MAGNETOM Cima.X are reportedly the strongest for currently available whole-body MRI scanners.
Offering a robust gradient system and a variety of workflow enhancements, the MAGNETOM Cima.X 3T whole-body magnetic resonance imaging (MRI) scanner has garnered 510(k) clearance from the Food and Drug Administration (FDA).
Siemens Healthineers, the manufacturer of the MAGNETOM Cima.X system, said the device features Gemini Gradients that have an amplitude of 200 millitesla per meter (mT/m) and a slew rate of 200 telsa per meter per second (T/m/s).
For imaging of patients with neurodegenerative diseases, the industry-leading gradient strength enhances the visibility of microstructures in the brain, according to Siemens Healthineers. The company noted that the MAGNETOM Cima.X system also features the artificial intelligence (AI)-powered Deep Resolve reconstruction technology, which can accelerate MRI brain scans by 70 percent.
The newly FDA-cleared, whole-body MAGNETOM Cima.X MRI system offers enhanced gradient strength that may facilitate improved visualization of brain microstructures as well as artificial intelligence (AI)-powered reconstruction technology that can accelerate MRI brain scans by 70 percent, according to Siemens Healthineers, the manufacturer of the system.
Another benefit of the whole-body MRI modality, according to Siemens Healthineers, is the capability to provide time-stamped physiological data through the system’s Physiologging feature, which enables clinicians to ascertain whether respiratory activity is compromising brain activity.
“With the FDA clearance of the MAGNETOM Cima.X, Siemens Healthineers proudly offers the scientific and medical communities a whole-body 3T MR scanner that can deliver penetrating new insights into oncologic, cardiac, and neurodegenerative disease,” noted Katie Grant, the vice president of magnetic resonance at Siemens Healthineers North America.
FDA Grants Expanded 510(k) Clearance for Xenoview 3T MRI Chest Coil in GE HealthCare MRI Platforms
November 21st 2024Utilized in conjunction with hyperpolarized Xenon-129 for the assessment of lung ventilation, the chest coil can now be employed in the Signa Premier and Discovery MR750 3T MRI systems.
FDA Clears AI-Powered Ultrasound Software for Cardiac Amyloidosis Detection
November 20th 2024The AI-enabled EchoGo® Amyloidosis software for echocardiography has reportedly demonstrated an 84.5 percent sensitivity rate for diagnosing cardiac amyloidosis in heart failure patients 65 years of age and older.
