The US Food and Drug Administration (FDA) has cleared two minimally invasive, catheter-based devices to create arteriovenous (AV) fistulas percutaneously in patients with chronic kidney disease who ...
The endoscopic device manufactured by Maquet was originally developed for harvesting of the saphenous vein and radial artery as conduits for coronary artery bypass graft surgery. These vessels are ...
- Humacyte plans to file a supplemental Biologic License Application (BLA) with the Food and Drug Administration (FDA) during the second half of 2026 - - The ATEV met V012’s primary endpoint and was ...
WASHINGTON--(BUSINESS WIRE)--The FDA-approved Ellipsys® Vascular Access System from Avenu Medical, Inc., became a key focus of attention throughout last week’s Controversies in Dialysis Access (CiDA) ...
Hundreds of patients living with chronic kidney disease across southern Jamaica gained improved access to haemodialysis ...
HUNDREDS of patients living with chronic kidney disease across southern Jamaica have gained improved access to haemodialysis ...
Repeated dialysis needling can cause painful aneurysmal fistulas that must be removed. A new, minimally invasive approach will decrease morbidity amonghemodialysis patients and help improve their ...
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