Welcome to our dedicated page for Koninklijke Phil news (Ticker: PHG), a resource for investors and traders seeking the latest updates and insights on Koninklijke Phil stock.
Koninklijke Philips N.V. (NYSE: PHG) is a global leader in health technology focused on improving lives through meaningful innovation. This news hub provides investors and healthcare professionals with centralized access to official press releases and verified updates about Philips' advancements in diagnostic imaging, connected care systems, and personal health solutions.
Discover timely information on product launches, regulatory milestones, and strategic partnerships that shape Philips' position in the healthcare sector. Our curated collection includes earnings reports, technology innovations, and market expansion announcements – all essential for understanding the company's trajectory in medical equipment and digital health solutions.
Key updates cover developments in AI-driven diagnostic tools, telehealth platforms, and sustainable healthcare initiatives. Bookmark this page to stay informed about Philips' progress in addressing critical challenges across radiology, cardiology, and home-based patient care through its integrated health technology ecosystem.
Philips (NYSE: PHG) unveiled its new CT 5100 – Incisive – featuring CT Smart Workflow at the RSNA annual meeting on November 29, 2021. This innovative technology uses artificial intelligence to streamline CT imaging processes, enhancing patient care while reducing operational costs. Key highlights include the Tube for Life guarantee, which could save up to USD 420,000 in lifetime operating costs. The CT Smart Workflow aims to improve efficiency and diagnostic confidence in radiology departments.
Royal Philips (NYSE: PHG) showcased its innovative portfolio of vendor-neutral radiology workflow solutions at the RSNA annual meeting from November 28 to December 2, 2021. The solutions focus on streamlining workflows for radiologists, technologists, and administrators through AI-driven informatics, enhancing diagnostic confidence and efficiency. Philips' new MR 5300 system, which received FDA 510(k) clearance, simplifies clinical tasks, while the company's commitment to sustainability is reinforced by its leadership in reducing CO2 emissions. Philips remains dedicated to improving healthcare outcomes and addressing workforce challenges in the radiology sector.
Philips has launched the world’s first spectral detector angio-CT solution at RSNA 2021, integrating breakthrough spectral CT imaging with real-time fluoroscopy. This innovative technology aims to enhance minimally invasive procedures in oncology, stroke, and trauma care. By combining the Spectral CT 7500 and Azurion with FlexArm, interventionalists gain immediate access to vital imaging modalities at the patient’s side, improving workflow and patient care. Philips is partnering with leading clinical institutions like Mayo Clinic to co-create this advanced imaging solution.
Royal Philips (NYSE: PHG) announced the launch of its new AI-powered MR 5300 and MR 7700 systems at the RSNA 2021 meeting. The MR 5300 system has received FDA 510(k) clearance and is designed for helium-free operations, enhancing sustainability and efficiency in outpatient clinics. The MR 7700 system features advanced multinuclear capabilities for improved imaging. Philips also introduced the AI-assisted MR Workspace, aimed at streamlining workflows and increasing productivity in radiology departments. The new portfolio emphasizes Philips' commitment to high-quality imaging and operational efficiency.
On November 22, 2021, Philips announced a collaboration with MedChat to integrate live chat and AI-driven chatbot services into its Patient Navigation Manager. This integration aims to enhance call center efficiency and expedite the resolution of patient inquiries in North America. The Patient Navigation Manager has shown significant success, with metrics indicating an 86% reduction in same-day cancellations and a 30% increase in referral conversions. The collaboration is part of Philips' commitment to improving patient management and outcomes through integrated health technology solutions.
Philips (NYSE: PHG) has received FDA 510(k) clearance for its Liver Fat Quantification tools integrated into the EPIQ Elite and Affiniti ultrasound systems. This advancement aims to enhance early-stage fatty liver disease diagnosis, which affects about 25% of the global population. The tools will be showcased at the Radiological Society of North America annual meeting. Philips emphasizes that improved diagnostic capabilities will lead to better patient outcomes, allowing for timely lifestyle changes to mitigate liver disease progression.
Royal Philips (NYSE: PHG) announced on November 14, 2021, that its subsidiary, Philips Respironics, is addressing potential health risks linked to foam in certain sleep and respiratory devices. The company initiated a voluntary recall in June 2021. The FDA recently inspected a manufacturing facility, providing observations that will be addressed by Philips. Testing continues on new silicone replacement foam, with results showing acceptable outcomes. Philips is committed to the health of affected patients and will share findings with authorities following ongoing assessments.
Philips has received a USD 15.4 million grant from the Bill & Melinda Gates Foundation to enhance its obstetrics app development for the handheld ultrasound device, Lumify. This project aims to improve maternal healthcare, particularly in underserved communities, targeting around 2.5 billion people by 2030, with a focus on reducing pregnancy-related deaths. The initiative will empower midwives in low-income areas with AI technology, enabling early identification of complications in pregnancy, ultimately aiming to decrease both maternal and fetal mortality rates.
Royal Philips (NYSE: PHG) announces results from a real-world analysis of Medicare data showing significant benefits of intravascular ultrasound (IVUS) in peripheral vascular interventions. Key findings include a 32% reduction in major adverse limb events like amputations during lower extremity interventions among over 697,794 patients and a 31% reduction in repeat interventions, hospitalizations, or deaths during iliofemoral venous stenting. The study emphasizes IVUS's potential to optimize patient care and improve long-term health outcomes.