Core Viewpoint - Berry Genomics (000710.SZ) has announced that its subsidiary, Hangzhou Berry Health and Technology Co., Ltd., has received the medical device registration certificate from the National Medical Products Administration (NMPA) for its third-generation sequencing instrument, Sequel?IICNDx, marking it as the first third-generation sequencing platform approved for clinical use globally [1] Group 1 - The Sequel?IICNDx instrument enables rapid implementation of third-generation sequencing solutions in local clinical laboratories, facilitating "multi-use" and "mixed operation" capabilities [1] - The approval of the Sequel?IICNDx is expected to reduce sample waiting times, accelerate report cycles, and enhance the quality and level of in-hospital services [1] - Berry Genomics has achieved full self-production of third-generation sequencing detection reagents and local deployment of an intelligent report interpretation system [1] Group 2 - The company provides comprehensive localized construction services for clinical processes, including sample collection and extraction, library construction, high-throughput sequencing, data analysis and interpretation, and report management [1]
贝瑞基因(000710.SZ):子公司三代基因测序仪SequelIICNDx获得医疗器械注册证