Infusion information collection system
- Device class
- Class III
- Model specifications
- MX8900-L、MX8900A-L
- Approval department
- State Drug Administration国家药品监督管理局
- Registration number
- 国械注准20243142503
- Approval date
- December 13, 2024
- Expiry date
- December 12, 2029
- Name
- Shenzhen Comen Medical Instruments Co., Ltd.深圳市科曼医疗设备有限公司
- Province/Region
- Guangdong广东
- Address
- A10-11 floors, 12C, 2 buildings, 1-5 floors, Building 1, FIYTA Watch Building, South Ring Avenue, Mashantou Community, Matian Street, Guangming District, Shenzhen深圳市光明区马田街道马山头社区南环大道飞亚达钟表大厦1栋A10层-11层、12C，2栋1-5层（一照多址企业）
- Production address
- 深圳市光明区马田街道南环大道飞亚达钟表大厦2栋1-5层、深圳市光明区马田街道富利南路与芳园路交汇处辉瑞大厦3楼、4楼北侧
产品与特定型号的输液泵、注射泵配合使用,为输液泵、注射泵供电,采集输液泵、注射泵数据并报警.
产品与特定型号的输液泵、注射泵配合使用，为输液泵、注射泵供电，采集输液泵、注射泵数据并报警。
产品由控制器、插件箱及附件(包括电源线、从控制器通讯电缆和接地线)组成.
产品由控制器、插件箱及附件（包括电源线、从控制器通讯电缆和接地线）组成。
- Appendix
- 产品技术要求
Access comprehensive regulatory information for Infusion information collection system in the China medical device market through Pure Global AI's free database. This Class III medical device is registered under NMPA registration number 国械注准20243142503 and owned by Shenzhen Comen Medical Instruments Co., Ltd.. The device was approved on December 13, 2024.
This page provides complete registration details including registrant information, province location (Guangdong), intended use, and regulatory compliance data from the official China NMPA medical device database. Pure Global AI offers free access to China's complete medical device registry, helping global MedTech companies navigate NMPA regulations efficiently.