Medical Device Purchasing Guide: A Comprehensive Analysis of Clinical Applicability and Compliance in 2026

This article systematically outlines the core essentials of current domestic medical equipment procurement, encompassing the latest registration requirements from the NMPA (formerly CFDA), clinical application scenario matching, acceptance standards for second-tier and above hospitals, and the trend of domestic substitution, aiming to assist medical institutions in making scientific decisions.

State Regulation: Decree No. 818

Regulations on the Administration of Clinical Research and Clinical Translational Application of New Biomedical Technologies Adopted at the 68th Executive Meeting of the State Council on 12 September 2025, and shall come into force on 1 May 2026.

Cell Industry Conference 2026