We need to provide a distinct range of labeled examples, including product information, device classifications, regulatory requirements, symbols ... contributions to the European Union Medical Device ...

For over four decades, the medical device industry has wrestled with fragmented data exchange and proprietary integrations.

WALTHAM, Mass., March 13, 2025--(BUSINESS WIRE)--Paragonix Technologies, a pioneer in organ transplant technologies and organ procurement services, announced today that five of its devices have ...

Medical Device Regulation 2017/745, commonly referred to as EU MDR. This approval further confirms Paragonix’s compliance with the highest quality control standards for medical devices and ...

Infusion pumps, glucose monitors, insulin pumps and dental implants were among the products with delayed side effect reporting TUESDAY, March 18, 2025 (HealthDay News) -- Other people could be ...

Given the calls for change, criticism, and ongoing consultations, this article sets out the current status of developments ...

the Company's compliance with medical device reporting regulations to report adverse events involving the Company's products, which could result in voluntary corrective actions or enforcement ...

LifeTech Scientific Corporation (the "Company" or "LifeTech", Stock code: 1302.HK), a company specializing in minimally ...