Both companies say the collaboration is driven by a shared mission to improve patient outcomes by aligning every step of the diagnostic process
The FDA classified LifeVac as a Class II medical device
Diasens and GlucoLive are designed for diabetic, Chronic Kidney Disease (CKD), and post-transplant patients who require continuous glycaemic surveillance and integrated remote care
The new equipment will be installed at Codis’ 400,000-square-foot Haverhill facility and is expected to be operational by 2027
Cognita CXR leverages a proprietary vision-language model to analyze full chest X-ray studies and generate comprehensive preliminary findings
Occlutech develops, manufactures, and commercialises medical devices for congenital heart disease, stroke prevention, and heart failure
The updated closure system introduces intuitive handling, innovative functionality and a premium design compatible with a wide range of syringe formats
The MAGiC catheter is designed for robotically-navigated cardiac ablation procedures
GlideTech materials are available in several standard base resins and offer customization options for specific applications
Syrma Johari is a globally recognised medical device engineering and manufacturing organisation
It performs white blood cell differential counts and quantifies red blood cell and platelet morphology,
Theracor is derived from human umbilical cord extracellular matrix (ECM) and is designed to cover, protect, and maintain a moist wound environment
The SAPIEN M3 transcatheter mitral valve replacement (TMVR) system is designed for patients with symptomatic moderate-to-severe or severe MR
Provides pain relief for more than 30 conditions, including chronic back pain, arthritis, and sports injuries
The system is intended for some of the tiniest patients—premature infants weighing as little as two pounds
The NP resin portfolio, indicated by its UL746G-certified prefix, equips manufacturers across industries to meet increasingly stringent regulatory and performance standards
The new site marks the company’s first operation in the region
Implementing PFAS testing in the early development stages allows medical device manufacturers to prepare for potential regulatory updates
The company introduced the ExcelSign E12 and E17 modular patient monitors, the Relife 1000 biphasic defibrillator, and a new OT charting software
The clearance for TELLTALE positions Transmural Systems at the forefront of next-generation electrosurgical solutions for structural heart interventions
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