GE HealthCare announces CE Mark for the Omni 128cm total body PET/CT system
28.11.2025 12:00:00 CET | Business Wire | Press Release
GE HealthCare today announced CE Mark for its next-generation Omni 128cm total body positron emission tomography / computed tomography (PET/CT) system,i a major milestone in its mission to advance precision care. Designed to advance cancer diagnosis, staging, therapeutic planning and treatment response monitoring, this innovative system represents a leap forward in molecular imaging capabilities and clinical efficiency.
As global cancer rates continue to rise – projected to increase 77 percent by 2050ii – the need for advanced imaging solutions has never been greater. The growing prevalence of cancer and emergence of investigational immunotherapies and targeted treatments have accelerated the demand for whole-body PET/CT imaging. GE HealthCare’s new technology is built to meet this need, supporting theranostics and enabling clinicians to visualize, diagnose and monitor disease with impressive precision and speed.
“Our commitment to precision health is rooted in innovation that also aims to anticipate the future of care,” says Jean-Luc Procaccini, President & CEO, Molecular Imaging and Computed Tomography, GE HealthCare. “With our Omni 128cm total body PET/CT system, we’re not just advancing imaging – we’re building a platform that empowers clinicians to deliver personalized, efficient and impactful care. The system also supports researchers in developing new clinical pathways. This milestone underscores our vision of enabling clinicians to achieve better outcomes through smarter, scalable solutions.”
The new PET/CT system is designed to accommodate head to thigh imaging in a single bed position for a wide range of patients –compared to traditional systems that typically require five-to-six bed positions – helping accelerate scan time and streamline workflows with intuitive artificial intelligence solutions to promote impressive clinical and operational efficiency. The system also enables ultra-low dose scans, multi-organ dynamic imaging as well as imaging of slow-decaying and low-activity tracers with the goal of enhancing both clinical practice and research, while improving operational efficiency across healthcare systems.
“PET/CT has transformed our ability to visualize disease at the cellular level, offering insights that were once out of reach,” shares Prof. Michael Hofman, nuclear medicine physician and head of the PET/CT program at Melbourne's Peter MacCallum Cancer Centre. “With the Omni 128cm total body PET/CT system, we’re entering a new phase of possibility – one where faster scans and broader imaging coverage could redefine how we approach translational research and accelerate the development of targeted therapies.”
The technology’s ultra-high sensitivity and excellent spatial resolution are designed to support imaging across a wide range of clinical applications, including the monitoring of advanced prostate cancer treatment. Its non-invasive nature and ability to quantify biological processes at the cellular level make it a powerful tool that can help in early disease identification and treatment planning.
“This next-generation PET/CT technology is engineered to deliver exceptional sensitivity and resolution – capabilities that could reshape how we approach molecular imaging,” adds Ken Herrmann, MD, director and chair, Department of Nuclear Medicine, Universitätsklinikum Essen. “Its speed and precision open the door to new possibilities, from helping reduce the need for anesthesia in pediatric scans to enabling multi organ dynamic imaging and early, confident diagnoses. It’s a powerful tool for advancing both research and patient care.”
In addition, the Omni 128cm PET/CT system supports advanced research applications – from developing new clinical pathways and novel PET tracers, to evaluating emerging theranostic agents – accelerating innovation from bench to bedside. When combined with GE HealthCare’s MIM software solutions, researchers and clinicians gain access to advanced quantitation tools and streamlined workflows that are not only important for helping enhance diagnostic confidence and operational efficiency, but also enable precise, personalized care that can help improve patient outcomes.
Furthermore, GE HealthCare’s Omni 128cm system leverages NVIDIA’s full stack accelerated computing platform technology to optimize the reconstruction process and reduce the time it takes to generate images and provide clinicians with the data necessary for fast, timely diagnoses.
2025 marks 25 years of PET/CT innovation at GE HealthCare. From launching the industry’s first commercially available PET/CT system, Discovery LS, to this introduction of a new total body PET/CT solution, GE HealthCare has consistently delivered innovative solutions to meet today and tomorrow’s most pressing needs. The company continues to drive a connected healthcare transformation, delivering integrated solutions that empower clinicians and help improve patient outcomes worldwide.
For more information on GE HealthCare’s molecular imaging portfolio, visit gehealthcare.com. Healthcare system representatives from CE Mark-observing countries are also invited to explore Omni 128cm in person at the Radiological Society of North America’s (RSNA) Annual Meeting in Chicago, November 30-December 3.
About GE HealthCare Technologies Inc.
GE HealthCare is a trusted partner and leading global healthcare solutions provider, innovating medical technology, pharmaceutical diagnostics, and integrated, cloud-first AI-enabled solutions, services and data analytics. We aim to make hospitals and health systems more efficient, clinicians more effective, therapies more precise, and patients healthier and happier. Serving patients and providers for more than 125 years, GE HealthCare is advancing personalized, connected and compassionate care, while simplifying the patient’s journey across care pathways. Together, our Imaging, Advanced Visualization Solutions, Patient Care Solutions and Pharmaceutical Diagnostics businesses help improve patient care from screening and diagnosis to therapy and monitoring. We are a $19.7 billion business with approximately 53,000 colleagues working to create a world where healthcare has no limits.
GE HealthCare is proud to be among 2025 Fortune World’s Most Admired Companies™.
Follow us on LinkedIn, X, Facebook, Instagram, and Insights for the latest news, or visit our website https://www.gehealthcare.com for more information.
i Omni with 128cm AFOV is CE marked. Available for sale in EU member states countries. Not approved or cleared by the U.S. FDA. Not available for sale in the U.S. and other non-EU member states countries.
ii Global cancer burden growing, amidst mounting need for services.” World Health Organization. Published 1 February 2024. Accessed 9 September 2024. https://www.who.int/news/item/01-02-2024-global-cancer-burden-growing--amidst-mounting-need-for-services
View source version on businesswire.com: https://www.businesswire.com/news/home/20251128007885/en/
Contacts
GE HealthCare Media Contact:
Margaret Steinhafel
M +1 608 381 8829
Margaret.Steinhafel@gehealthcare.com
(c) 2024 Business Wire, Inc., All rights reserved.
Business Wire, a Berkshire Hathaway company, is the global leader in multiplatform press release distribution.
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
BeOne Presents Compelling Data in Hard-to-Treat Liver and Lung Cancers at ESMO 202624.10.2026 10:15:00 CEST | Press Release
BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced new data from multiple differentiated investigational medicines across its priority solid tumor disease areas at the European Society for Medical Oncology (ESMO) Congress 2026 (October 23–27, Madrid). The presentations span gastrointestinal, lung, and breast cancers, and reflect the growing momentum of BeOne’s solid tumor franchise. Mark Lanasa, M.D., Ph.D., Chief Medical Officer, Solid Tumors at BeOne, said: “At ESMO, we are showing how our strategy of matching the right modality to disease biology is translating into meaningful clinical progress. Our GPC3 x 4-1BB bispecific antibody continues to be well tolerated and demonstrates durable activity with longer follow up in patients with heavily pre-treated hepatocellular carcinoma, while the first clinical data from our brain-penetrant PRMT5 inhibitor and CEA-targeting ADC expand our innovation in non-small cell lung cancer. Alongsi
Phase 3 RAINIER Results Supporting Best-in-Class Potential of Povetacicept in IgA Nephropathy Published in the New England Journal of Medicine and Presented at the American Society of Nephrology Kidney Week 202623.10.2026 19:42:00 CEST | Press Release
Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) today announced the publication of Phase 3 RAINIER results for povetacicept in the New England Journal of Medicine (NEJM), presentation of these data at the American Society of Nephrology (ASN) Kidney Week 2026 in Denver, Colorado, and advancement of the povetacicept clinical research program in IgAN. Vertex will also host an investor event during ASN on October 23 at 6:15-7 p.m. MDT (8:15-9 p.m. EDT). Further details are below. Data being presented include a pre-specified Week 36 interim analysis of the ongoing Phase 3 RAINIER trial of povetacicept, an engineered fusion protein and dual inhibitor of the BAFF (B cell activating factor) and APRIL (a proliferation inducing ligand) cytokines, in immunoglobulin A nephropathy (IgAN). RAINIER met its primary endpoint, with povetacicept achieving a 52.0% reduction from baseline in proteinuria at Week 36 and a statistically significant and clinically meaningful 49.8% reduction versus placebo (
Lifezone Metals Confirms Advanced Negotiations with Orion CMC on Kabanga Nickel Project23.10.2026 16:19:00 CEST | Press Release
Lifezone Metals Limited (NYSE: LZM) notes comments made today by Oskar Lewnowski, Founder and Group Chief Executive of Orion Resource Partners, in an interview with Bloomberg Television regarding the Company’s Kabanga Nickel Project in Tanzania. In response to inbound inquiries from media outlets and investors following the interview, the Company can confirm that negotiations with Orion Critical Mineral Consortium (Orion CMC) regarding a significant equity investment into the Kabanga Nickel Project are at an advanced stage. The Orion CMC is a global investment platform launched by Orion Resource Partners in partnership with the U.S. International Development Finance Corporation (DFC) and Abu Dhabi's sovereign investor ADQ. As previously announced, the Company has been running a competitive process, led by Standard Chartered Bank, to secure a strategic investment into the Kabanga Nickel Project. Social Media LinkedIn | X | YouTube About Lifezone Metals Lifezone Metals (NYSE: LZM) is com
BeOne Medicines Reports Sustained Survival Benefit with TEVIMBRA-ZIIHERA Combination in First-Line HER2+ Gastroesophageal Cancer23.10.2026 16:15:00 CEST | Press Release
BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced new survival results from the planned second interim analysis (IA2) and final formal analysis of the Phase 3 HERIZON-GEA-01 trial, further confirming the benefit of TEVIMBRA® (tislelizumab) plus ZIIHERA® (zanidatamab) and chemotherapy as first-line treatment for patients with HER2-positive locally advanced or metastatic gastroesophageal adenocarcinoma (GEA). The results will be presented today as a late-breaking abstract during a rapid oral session at the European Society for Medical Oncology (ESMO) Congress 2026 in Madrid, Spain (LBA79). Mark Lanasa, M.D., Ph.D., Chief Medical Officer, Solid Tumors at BeOne, said: “Following the U.S. approval in August, these longer-term data provide further evidence supporting TEVIMBRA plus ZIIHERA and chemotherapy as the new standard of care in all first-line HER2-positive advanced gastroesophageal adenocarcinoma patients, regardless of PD-L1 sta
inDrive and Pony.ai Announce Collaboration to Explore Autonomous Mobility in Kazakhstan Built on NVIDIA Hyperion23.10.2026 15:00:00 CEST | Press Release
inDrive, the global mobility and delivery platform, today announced it has signed a memorandum of understanding (MOU) with NVIDIA and Pony.ai, a global leader in the large-scale commercialization of autonomous driving technology, to explore the future of autonomous ride-hailing. Kazakhstan will serve as the first test market. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20261023143469/en/ inDrive partners with Pony.ai and NVIDIA to explore autonomous mobility in Kazakhstan Kazakhstan was chosen first for its regulatory readiness following the creation of the country’s first structured legal framework for driverless transport, as part of its “Year of Digitalization and Artificial Intelligence.” Combined with Kazakhstan’s position as a leading Central Asian economy, this gives the companies a clear basis to assess autonomous ride-hailing in practice. The three companies will evaluate the technical, operational, regulatory and
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom