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爱威科技10月9日获融资买入430.43万元,融资余额4796.05万元
Xin Lang Cai Jing· 2025-10-10 01:28
截至6月30日,爱威科技股东户数4086.00,较上期增加13.34%;人均流通股16642股,较上期减少 11.77%。2025年1月-6月,爱威科技实现营业收入1.10亿元,同比增长12.70%;归母净利润1405.54万 元,同比增长21.16%。 10月9日,爱威科技跌1.51%,成交额3703.27万元。两融数据显示,当日爱威科技获融资买入额430.43 万元,融资偿还334.34万元,融资净买入96.09万元。截至10月9日,爱威科技融资融券余额合计4796.05 万元。 融资方面,爱威科技当日融资买入430.43万元。当前融资余额4796.05万元,占流通市值的2.76%,融资 余额超过近一年80%分位水平,处于高位。 融券方面,爱威科技10月9日融券偿还0.00股,融券卖出0.00股,按当日收盘价计算,卖出金额0.00元; 融券余量0.00股,融券余额0.00元,超过近一年90%分位水平,处于高位。 资料显示,爱威科技股份有限公司位于湖南省长沙市岳麓区学士街道茯苓路26号爱威医疗科技园,成立 日期2000年3月16日,上市日期2021年6月16日,公司主营业务涉及医疗临床检验分析仪器及配套体外 ...
第一上海:维持国药控股“买入”评级 目标价21.3港元
Zhi Tong Cai Jing· 2025-09-29 06:25
医药分销板块方面,期内营业收入为2,185.3亿元,同比下降3.52%。经营溢利率为2.58%,较上年同期 下降0.17个百分点,主要受终端销售价格下降和院端品类结构调整影响。2025年H1国谈品种销售额保持 快速增长,销售收入及毛利额同比均实现双位数增长。渠道结构上,国药控股积极推进等级医院核心市 场品种增长,同时紧抓基层医疗市场刚需,带动整体份额增长。收入下降也部分由于公司主动的战略转 型,降低低毛利、低周转的收入占比,推动行业供应链效率和合规提升,持续挖掘新环境下业务可持续 增长的能力。 器械分销业务来看,实现收入570.5亿元,同比下滑2.46%。经营溢利率为1.92%,同比下降0.33个百分 点,主要是高毛利器械收入占比降低以及行业配送毛利率整体下行所致。医疗设备与IVD品类销售呈现 明显回落,而医用耗材保持稳健增长。公司主动收缩长账期、低附加值及资金占用较高的业务规模,持 续优化渠道结构,上半年净新增SPD项目7个、单体医院集中配送项目18个及医联体、医共体集中配送 项目1个。SPD项目带动器械收入同比增长13%。此外,公司新增35项服务类软件著作权,进一步赋能 终端医院运营。 此外,医药零售板块 ...
第一上海:维持国药控股(01099)“买入”评级 目标价21.3港元
智通财经网· 2025-09-29 06:24
智通财经APP获悉,第一上海发布研报称,维持国药控股(01099)"买入"评级,目标价21.3港元。国药控 股作为医药流通行业龙头,短期业绩虽承压,但零售板块逆势增长与国大药房扭亏初显转型成效。长期 仍受益于老龄化趋势与集约化政策,预计公司将逐步走出之前调整带来的业务转型压力。 报告中称,国药控股2025年上半年实现营业收入2,860.4亿元,较去年同期下降2.95%。毛利为203.5亿 元,同比下降7.28%。整体毛利率持续承压,上半年为7.11%,同比下降了0.34%。净利润为53.37亿元, 同比下降9.53%。归属于公司权益持有人的利润为34.7亿元,同比下降6.43%。费用管控成效显著,销 售、管理和财务费用率分别降至2.74%、1.28%和0.35%,主因融资成本降低、一体化整合深化及业务成 本优化。期间费用率下降有效缓解利润压力,推动利润率同比降幅收窄,报告期内利润率为1.21%,同 比下降3.59个百分点。 医药分销板块方面,期内营业收入为2,185.3亿元,同比下降3.52%。经营溢利率为2.58%,较上年同期 下降0.17个百分点,主要受终端销售价格下降和院端品类结构调整影响。2025年H ...
美国对机器人、机械和医疗设备启动232调查
Xin Lang Cai Jing· 2025-09-24 20:56
根据《联邦公报》发布的通知,美国商务部对机器人、工业机械、医疗设备、医用耗材以及个人防护设 备的进口展开调查。 ...
事关创新药械全生命周期价值评估,年底前11省份启动这项试点
Di Yi Cai Jing· 2025-09-23 07:53
"真实世界医保综合价值评价"将挂钩医保商保"双目录"调整 真实世界研究驱动医药创新再进一步。 23日,国家医保局发布"关于开展真实世界医保综合价值评价试点工作的通知"(以下简称"通知")。根据通知,未来三年里,我国将通过 试点探索,形成一套"以价值为导向、基于真实世界研究的医保综合价值评价体系"。2027年年底,该评价体系将进入"全国范围推广"阶 段。 目前,北京、海南、江苏等11省已被纳入试点范围。接下来,国家医保局将对试点先行地区进行动态管理,确保"有进有出"。 具体来说,在药品领域的应用场景有7个,分别为上市前研发立项参考、药品首发挂网、医保及商保创新药目录调整、集采药品疗效及价 格分析、挂网药品价格治理、药品使用分析(用法用量、联合用药、超适应症用药等)和上市后药品价值再评价。 在医用耗材领域应用场景有5个,分别为(异地就医)医用耗材医保目录调整、可单独收费目录调整、医用耗材挂网及价格治理、创新医用 耗材医保分类和集采医用耗材分组及比价系数调整。 这一基于真实世界证据的医保综合价格评价体系有望影响创新药、仿制药、医用耗材和医疗服务的定价、价格调整和多层次支付保障。根 据通知,该评价体系会在药品首发挂网 ...
爱威科技股价跌5.25%,诺安基金旗下1只基金位居十大流通股东,持有47.74万股浮亏损失63.97万元
Xin Lang Cai Jing· 2025-09-23 02:41
资料显示,爱威科技股份有限公司位于湖南省长沙市岳麓区学士街道茯苓路26号爱威医疗科技园,成立 日期2000年3月16日,上市日期2021年6月16日,公司主营业务涉及医疗临床检验分析仪器及配套体外诊 断试剂、医用耗材的研发、生产、销售和服务。主营业务收入构成为:试剂45.63%,仪器34.53%,耗 材17.56%,其他(补充)2.28%。 从爱威科技十大流通股东角度 数据显示,诺安基金旗下1只基金位居爱威科技十大流通股东。诺安多策略混合A(320016)二季度新 进十大流通股东,持有股数47.74万股,占流通股的比例为0.7%。根据测算,今日浮亏损失约63.97万 元。连续3天下跌期间浮亏损失43.44万元。 诺安多策略混合A(320016)成立日期2011年8月9日,最新规模13.99亿。今年以来收益57.56%,同类 排名694/8172;近一年收益115.52%,同类排名360/7995;成立以来收益204.1%。 9月23日,爱威科技跌5.25%,截至发稿,报24.19元/股,成交1359.59万元,换手率0.81%,总市值16.45 亿元。爱威科技股价已经连续3天下跌,区间累计跌幅3.44%。 诺 ...
30天支付!医院回款机制进入快车道
思宇MedTech· 2025-09-22 04:20
Core Viewpoint - The article discusses the recent draft regulation by the Sichuan Provincial Medical Security Bureau aimed at improving the online settlement process for drug and medical consumables procurement, which is expected to shorten payment cycles and enhance the efficiency of medical insurance fund usage [2][3]. Group 1: Policy Background and Overall Goals - The draft regulation builds on the 2020 interim measures and addresses issues such as long payment cycles and financial pressure on hospitals and companies due to the implementation of centralized procurement [3][4]. - The main goal of the draft regulation is to refine existing policies and respond to the national trend of reforming medical insurance fund settlement [3][4]. Group 2: Settlement Mechanism for Centralized Procurement Products - The draft regulation establishes a systematic settlement mechanism for centralized procurement products, which includes a prepayment and phased payment model [4][8]. - Medical institutions must sign a prepayment agreement with the medical insurance agency, which will provide an initial payment of at least 50% of the contract amount within 15 working days of signing [7]. - This model ensures cash flow for companies during the initial supply phase and provides financial relief for hospitals, thereby reducing uncertainty in payment cycles [8][11]. Group 3: Non-Centralized Procurement Consumables Settlement - The draft regulation specifies a 30-day payment timeline for non-centralized procurement consumables, a significant improvement over previous payment cycles that could extend for months [13][15]. - This change aims to facilitate quicker cash recovery for non-centralized products under the new regulatory framework [15]. Group 4: Institutional Innovations - The draft regulation enhances the role of the regulatory account, which acts as a secure channel for all payments, ensuring that funds are managed safely and efficiently [17][20]. - A monthly reconciliation mechanism is mandated, requiring the provincial procurement service center to send transaction summaries to all parties involved within the first five working days of each month [18][33]. Group 5: National Policy Trends and Sichuan Characteristics - The Sichuan draft regulation aligns with national efforts to expedite payment processes for medical consumables, reflecting a broader trend in healthcare reform [40]. - The regulation combines national reform directions with local practical experiences, showcasing its forward-looking and feasible nature [40]. Group 6: Industry Impact and Multi-Party Benefits - The policy adjustments are expected to yield multiple positive effects for the industry, particularly by providing special support for innovative drugs, allowing direct settlements between medical insurance funds and companies [41]. - This approach emphasizes the importance of innovation in drug development and aims to facilitate the entry of more innovative products into clinical applications [41]. Group 7: Conclusion - The ongoing optimization of the payment mechanism in Sichuan reflects the overall direction of national medical insurance payment reforms, aiming to create an efficient financial flow among hospitals, medical insurance, and companies [42]. - The improvements in payment timelines for both centralized and non-centralized products indicate a gradual resolution of the "slow payment" dilemma, promoting a more efficient, transparent, and standardized settlement process [42].
稳健医疗:约4.07亿股限售股9月17日解禁
Mei Ri Jing Ji Xin Wen· 2025-09-12 11:05
Group 1 - The company,稳健医疗, announced that approximately 407 million restricted shares will be unlocked and listed for trading on September 17, 2025, representing about 69.83% of the total share capital [1] - For the first half of 2025, the revenue composition of the company is as follows: health lifestyle consumer products account for 51.84%, medical consumables account for 47.49%, and other businesses account for 0.67% [1] - As of the report date, the market capitalization of the company is 22.8 billion yuan [1]
天津出台基本医保医用耗材目录 收录3062种医用耗材
Yang Shi Xin Wen· 2025-09-05 08:57
Core Points - The Tianjin Municipal Medical Insurance Bureau has issued the "Tianjin Basic Medical Insurance Medical Consumables Directory (2025)", which will be officially implemented on September 18, 2025 [1] - The directory aims to enhance the precision, scientific management, and standardization of medical consumables reimbursement under the medical insurance system, ensuring that insured patients receive their entitled benefits [1] Summary by Categories - **Reimbursement Scope**: The directory specifies the reimbursement range for medical consumables applicable to Tianjin's basic medical insurance and maternity insurance, currently including 3,062 types of medical consumables [1] - **Classification Management**: The consumables in the directory are categorized into two classes: Class A with 1,896 types and Class B with 1,166 types [1] - **Support for Innovation**: The directory supports technological innovation in the pharmaceutical industry and will implement dynamic adjustments with a "dynamic entry and exit" policy for consumables [1] - **Policy Clarity**: The compilation of the directory aims to clarify the range of consumables eligible for medical insurance payment, reasonably determine reimbursement standards, and gradually transition towards more refined management, aiding medical institutions in policy understanding and execution [1]
医疗器械出海深度(一)欧洲市场:高壁垒但可突破,未来中国企业销售有望提速
Changjiang Securities· 2025-09-02 09:46
Investment Rating - The report maintains a "Positive" investment rating for the medical device industry [14]. Core Insights - The European market is a core market for global medical devices, with a market size of approximately €160 billion in 2023, growing by 2.4% year-on-year. The global medical device market reached $582.6 billion in 2023, with Europe accounting for about 26% of the total market share [4][9]. - The report emphasizes that European medical device companies should focus on direct sales strategies in key markets such as Germany, France, and the UK, while utilizing distributors in other regions to penetrate the market [10][11]. - Chinese medical device companies are expected to accelerate their sales in Europe, leveraging their cost advantages and localizing their teams to adapt to the market [12][11]. Summary by Sections European Market Overview - Europe is the second-largest medical device market globally, with a stable growth rate and a concentration of market share among the top five countries: Germany, France, Italy, the UK, and Spain, which together account for 66% of the market [9][34]. - The average healthcare expenditure in Europe is about 11% of GDP, with approximately 7.9% allocated to medical technology [9][27]. Regulatory Environment - The report highlights the increased difficulty in obtaining regulatory approval under the new EU Medical Device Regulation (MDR), with costs for certification reaching approximately €4.25 million for medical devices and €2.34 million for in vitro diagnostics (IVD) [10][58]. - The certification process is lengthy, with an average duration of 1.5 to 2 years for mature technologies [10][58]. Sales Strategies - The report suggests that companies should prioritize direct sales in the UK, France, and Germany, while using distributors in other regions due to language barriers and varying regulatory environments [10][65]. - Distributors are increasingly providing comprehensive solutions, integrating product supply, technical services, training, and customer relationship management [10][73]. Market Opportunities for Chinese Companies - Chinese medical device companies are making inroads into the European market, with strategies including establishing local teams and partnerships to enhance market penetration [11][96]. - The report identifies that the medical consumables segment is the primary focus for Chinese exports to Europe, accounting for 49% of the total export value [125][130].