Review on Global Regulatory Landscape of Unique Device Identification (Udi) in Medical Device

The Unique Device Identification (UDI) system is a widely accepted access uniquely determining medical apparatus, boosting post-market surveillance, and improving patient safety.This review article comprehensively examines the landscape surrounding UDI implementation in different countries.With an increasing focus on the harmonization of medical device regulations, this study offers insights into the similarities and disparities in UDI adoption across various regions.The analysis encompasses key aspects of UDI implementation, including regulatory requirements, timelines for compliance, data standards, and enforcement mechanisms.The review covers major markets like the United States, European Union, India, and Global IMDRF countries.It critically evaluates the UDI systems strengths, challenges, and impacts on the healthcare industry and regulatory authorities.Furthermore, the article highlights successful case studies of countries that have effectively integrated UDI into their healthcare systems, leading to improved traceability, reduced counterfeiting, and enhanced patient outcomes.Additionally, it examines the complexities associated with implementing UDI requirements in diverse healthcare settings, such as resourceconstrained environments.On completion, this review article presents a comprehensive overview of the regulatory landscape of Unique Device Identification for medical devices in different countries.It emphasizes the importance of continued efforts toward standardization, collaboration,