BERRY GENOMICS(000710)
Search documents
医疗服务板块11月5日跌0.34%,百诚医药领跌,主力资金净流出8.47亿元
Zheng Xing Xing Ye Ri Bao· 2025-11-05 08:48
证券之星消息,11月5日医疗服务板块较上一交易日下跌0.34%,百诚医药领跌。当日上证指数报收于 3969.25,上涨0.23%。深证成指报收于13223.56,上涨0.37%。医疗服务板块个股涨跌见下表: | 代码 | 名称 | 收盘价 | 涨跌幅 | 成交量(手) | 成交额(元) | | | --- | --- | --- | --- | --- | --- | --- | | 688710 | 益诺思 | 45.33 | 4.93% | 1.89万 | | 8372.51万 | | 000710 | 贝瑞基因 | 14.13 | 4.20% | 47.97万 | | 6.91亿 | | 002219 | 新里程 | 2.33 | 2.19% | 104.75万 | | 2.44亿 | | 688202 | 美迪西 | 67.19 | 1.30% | - 3.55万 | | 2.36亿 | | 301060 | 兰卫医学 | 9.87 | 0.82% | 5.45万 | | 5363.17万 | | 301239 | 普瑞眼科 | 37.30 | 0.78% | 1.02万 | | 3795.71万 | ...
PacBio Supports Berry Genomics in Achieving First Regulatory Approval for Clinical Long-Read Sequencing in China
Globenewswire· 2025-11-04 14:05
Core Insights - The Sequel II CNDx system has received Class III Medical Device Registration approval from the National Medical Products Administration (NMPA) in China, enabling the use of PacBio HiFi sequencing for complex genetic conditions, starting with thalassemia [1][2] - This approval represents the world's first regulatory clearance for a clinical-grade long-read sequencer, marking a significant advancement in precision medicine and genomic testing in China [2] - The Sequel II CNDx system allows clinicians to obtain a comprehensive view of the genome in a single test, accurately capturing various genetic variants [3] Company Developments - The approval of the Sequel II CNDx system, in conjunction with Berry Genomics' clinical thalassemia assay, establishes the first end-to-end long-read sequencing workflow for hospitals and diagnostic labs in China [4] - PacBio's technology utilizes Single Molecule, Real-Time (SMRT) technology, which is capable of delivering high accuracy and long read lengths of 20 kb and greater, enhancing the analysis of DNA molecules [5] - Berry Genomics plans to expand its capabilities to include additional clinical assays for various genetic disorders, demonstrating a commitment to improving diagnostic accuracy [6] Industry Impact - The NMPA approval signifies a major advancement for China's clinical genomics ecosystem, allowing for in-country testing with reduced turnaround times and improved diagnostic yield compared to existing technologies [6] - As demand for comprehensive genomic testing increases, PacBio aims to enhance the clinical utility of HiFi sequencing through partnerships and investments in AI-powered analysis [6] - The collaboration between PacBio and Berry Genomics reflects a shared vision to provide clinicians with accurate and comprehensive genomic insights, potentially transforming patient care [6]
精准医疗板块11月4日跌1.77%,透景生命领跌,主力资金净流出9.79亿元
Sou Hu Cai Jing· 2025-11-04 08:57
Market Overview - The precision medicine sector experienced a decline of 1.77% on November 4, with TuoJing Life leading the drop [1][2] - The Shanghai Composite Index closed at 3960.19, down 0.41%, while the Shenzhen Component Index closed at 13175.22, down 1.71% [1] Stock Performance - Notable stock performances in the precision medicine sector included: - RenDu Bio (688193) closed at 52.90, up 1.05% with a trading volume of 7076.23 hands and a transaction value exceeding 36.99 million yuan [1] - TuoJing Life (300642) closed at 22.73, down 2.86% with a trading volume of 78,200 hands and a transaction value of 178 million yuan [2] - Other companies like DaAn Gene (002030) and Anke Bio (300009) showed minimal changes, with DaAn Gene remaining flat at 6.57 and Anke Bio down 0.55% to 10.84 [1][2] Capital Flow - The precision medicine sector saw a net outflow of 979 million yuan from institutional investors, while retail investors contributed a net inflow of 642 million yuan [2][3] - Specific stock capital flows indicated: - GuoMai Technology (002093) had a net inflow of 8.61 million yuan from institutional investors, while retail investors saw a net outflow of 15.98 million yuan [3] - TuoJing Life experienced minimal net inflow from institutional investors at 25,000 yuan, with retail investors also showing a slight outflow [3]
医疗服务板块11月3日跌0.59%,数字人领跌,主力资金净流出7.12亿元
Zheng Xing Xing Ye Ri Bao· 2025-11-03 08:47
Market Overview - The medical services sector experienced a decline of 0.59% on November 3, with "Digital Human" leading the drop [1] - The Shanghai Composite Index closed at 3976.52, up 0.55%, while the Shenzhen Component Index closed at 13404.06, up 0.19% [1] Top Performers in Medical Services - Baicheng Pharmaceutical (301096) saw a significant increase of 19.15%, closing at 68.99 with a trading volume of 312,000 shares and a transaction value of 2.061 billion [1] - Berry Genomics (000710) rose by 6.11%, closing at 13.89 with a trading volume of 493,700 shares and a transaction value of 690 million [1] - YaoKang Bio (688046) increased by 4.77%, closing at 18.67 with a trading volume of 82,900 shares and a transaction value of 154 million [1] Underperformers in Medical Services - Digital Human (920670) led the decline with a drop of 6.20%, closing at 17.70 with a trading volume of 153,800 shares and a transaction value of 272 million [2] - Yixin Information (688710) fell by 5.70%, closing at 44.68 with a trading volume of 27,400 shares and a transaction value of 123 million [2] - Haoyuan Pharmaceutical (688131) decreased by 5.50%, closing at 75.40 with a trading volume of 79,400 shares and a transaction value of 601 million [2] Capital Flow Analysis - The medical services sector experienced a net outflow of 712 million from institutional investors, while retail investors saw a net inflow of 466 million [2][3] - Berry Genomics (000710) had a net inflow of 152 million from institutional investors, but a net outflow of 68.58 million from retail investors [3] - Baicheng Pharmaceutical (301096) recorded a net inflow of 124 million from institutional investors, with a net outflow of 99.78 million from retail investors [3]
突发!70亿机器人概念股与富士康汽车拟合作部署不低于2000台具身智能机器人
Xin Lang Cai Jing· 2025-10-31 12:38
Company Highlights - Tianqi Co., Ltd. signed a strategic cooperation framework agreement with Foxconn Automotive, planning to deploy no less than 2,000 embodied intelligent robots in the next five years [1] - Tianhua New Energy's actual controllers plan to transfer 12.95% of shares to CATL at a price of 24.49 yuan per share, which is a 19% discount compared to the closing price [2] - Zhenyu Technology plans to invest 21.1 billion yuan in humanoid robot precision module and component projects [3] - Taiyuan Heavy Industry disclosed false financial data in its annual report, leading to a change in its stock name to "ST Tai Heavy" starting November 4 [4] Investment & Contracts - East Asia Machinery plans to invest 400 million yuan to build an intelligent manufacturing base for air compressors and core components in Central China [12] Shareholding Changes - TuoStar's director plans to reduce his holdings by up to 0.95% [14] - Shanghai Fosun Pharmaceutical plans to reduce its holdings in Shanhe Pharmaceutical by up to 3% [16] Business Performance - Pingzhi Information reported a total procurement amount of 469 million yuan for server-related products since May [17] - Berry Genomics received medical device registration for the world's first clinically approved third-generation sequencing platform, Sequel® IICNDx [18] Contracts & Project Awards - Hopu Co., Ltd. signed a 5.2 billion yuan procurement contract for a storage system [20] - Qiaoyin Co., Ltd. received a bid notification for a 5.12 billion yuan urban sanitation integration project [20] Stock Price Movements - Hezhong China experienced a 46.56% increase in stock price over four consecutive trading days, indicating potential irrational speculation [22] Other Announcements - Huaxin Cement will change its stock name to Huaxin Building Materials starting November 6 [23]
贝瑞基因子公司三代基因测序仪SequelII CNDx获得医疗器械注册证
Zhi Tong Cai Jing· 2025-10-31 11:04
Core Insights - Berry Genomics (000710.SZ) 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 II CNDx, marking it as the first clinically approved third-generation sequencing platform globally [1][2] Group 1: Product Approval and Features - The Sequel II CNDx is the first third-generation sequencing platform approved for clinical use, enabling rapid implementation of third-generation sequencing solutions in local laboratories [1] - The approval allows for "one machine, multiple uses" and "mixed loading," which reduces sample waiting times, accelerates report cycles, and enhances service quality within hospitals [1] Group 2: Clinical Applications and Impact - The clinical approval of Sequel II CNDx will enhance the birth defect prevention system and significantly improve the detection capabilities for complex single-gene diseases [2] - Berry Genomics aims to deepen the clinical application of third-generation sequencing technology by optimizing AI algorithms and local deployment plans, making testing services more precise, efficient, and economical for families [2] - The large-scale application of third-generation sequencing technology is expected to accelerate major public health initiatives, such as the prevention of birth defects, both in China and globally [2]
贝瑞基因子公司三代基因测序仪Sequel®II CNDx获得医疗器械注册证
Zhi Tong Cai Jing· 2025-10-31 10:47
Group 1 - Berry Genomics' subsidiary, Hangzhou Berry Genomics and Health Technology Co., Ltd., has received the NMPA medical device registration certificate for its third-generation sequencing instrument, Sequel® II CNDx, making it the first clinically approved third-generation sequencing platform globally [1] - The approval of Sequel® II CNDx enables rapid implementation of third-generation sequencing solutions in local clinical laboratories, reducing sample waiting times, accelerating report cycles, and enhancing service quality within hospitals [1] - Berry Genomics has achieved full self-production of third-generation sequencing testing reagents and the local deployment of an intelligent report interpretation system, providing comprehensive localized services from sample collection to report management [1] Group 2 - The clinical approval of Sequel® II CNDx enhances the birth defect prevention system and significantly improves the detection capabilities for complex single-gene diseases [2] - Berry Genomics aims to deepen the clinical application of third-generation sequencing technology by optimizing AI algorithms and local deployment plans, making testing services more precise, efficient, and economical for families [2] - The large-scale application of third-generation sequencing technology is expected to accelerate the advancement of major public health projects, such as birth defect prevention, both in China and globally [2]
贝瑞基因子公司三代基因测序仪Sequel II CNDx获得医疗器械注册证
Zhi Tong Cai Jing· 2025-10-31 10:46
Group 1 - The core point of the article is that Berry Genomics' subsidiary has received regulatory approval for its third-generation gene sequencer, Sequel II CNDx, marking it as the first clinically approved platform of its kind globally [1][2] - The approval allows for the rapid implementation of third-generation sequencing solutions in local clinical laboratories, enhancing service quality and reducing sample wait times [1] - Berry Genomics has achieved full local production of third-generation sequencing reagents and the deployment of an intelligent report interpretation system, providing comprehensive localized services from sample collection to report management [1] Group 2 - The clinical approval of Sequel II CNDx will improve the birth defect prevention system and enhance the detection capabilities for complex single-gene diseases [2] - The company aims to further develop the clinical applications of third-generation sequencing technology by optimizing AI algorithms and local deployment plans, making testing services more accessible and cost-effective for families [2] - The large-scale application of third-generation sequencing technology is expected to significantly advance major public health initiatives, such as the prevention of birth defects, both in China and globally [2]
贝瑞基因(000710.SZ)子公司三代基因测序仪Sequel®II CNDx获得医疗器械注册证
智通财经网· 2025-10-31 10:45
Core Insights - Berry Genomics' subsidiary, Hangzhou Berry Genomics, has received NMPA approval for its Sequel® II CNDx third-generation gene sequencer, marking it as the first clinically approved third-generation sequencing platform globally [1][2] - The approval allows for rapid implementation of third-generation sequencing solutions in local clinical laboratories, enhancing service quality and reducing sample wait times [1] - Berry Genomics has achieved full local production of third-generation sequencing reagents and the deployment of an intelligent report interpretation system, providing comprehensive localized services from sample collection to report management [1] Industry Impact - The clinical approval of Sequel® II CNDx will enhance the birth defect prevention system and significantly improve the detection capabilities for complex single-gene diseases [2] - The advancement of domestic technology is expected to accelerate its global reach, with Berry Genomics aiming to optimize AI algorithms and local deployment plans to lower technical barriers [2] - The large-scale application of third-generation sequencing technology is anticipated to promote significant public health initiatives, particularly in the prevention of birth defects both in China and globally [2]
贝瑞基因:三代基因测序仪Sequel II CNDx获得医疗器械注册证
Zheng Quan Shi Bao Wang· 2025-10-31 10:08
Core Viewpoint - Berry Genomics (000710) announced that its wholly-owned subsidiary, Hangzhou Berry Genomics and Health Technology Co., Ltd., has recently received the medical device registration certificate from the National Medical Products Administration (NMPA) for its third-generation gene sequencer, Sequel II CNDx [1] Group 1 - The Sequel II CNDx is a third-generation gene sequencer [1] - The medical device registration certificate was issued by the National Medical Products Administration (NMPA) [1]