Intermittent pulse pressure antithrombotic system
- Device class
- Class II
- Model specifications
- VP-800、VP-600、VP-300
- Approval department
- Guangdong Provincial Drug Administration广东省药品监督管理局
- Registration number
- 粤械注准20242090830
- Approval date
- June 25, 2024
- Expiry date
- June 24, 2029
- Name
- Shenzhen Lifotronic Technology Co., Ltd.深圳普门科技股份有限公司
- Province/Region
- Guangdong广东
- Address
- Pumen Science and Technology Headquarters Building, No. 8, Qiuzhi East Road, Guancheng Community, Guanhu Street, Longhua District, Shenzhen深圳市龙华区观湖街道观城社区求知东路8号普门科技总部大厦
- Production address
- 广东省东莞市松山湖园区彰化路2号1号厂房2-11楼（委托生产）
It is suitable for the adjuvant treatment of limb dysfunction caused by cerebrovascular accident, brain trauma, brain surgery, spinal cord lesions, as well as the prevention of venous thrombosis and the reduction of limb edema.
适用于脑血管意外、脑外伤、脑手术后、脊髓病变引起的肢体功能障碍的辅助治疗，以及预防静脉血栓形成，减轻肢体水肿。
It consists of a main unit, an inflatable extension hose and an air bag.
由主机、充气延长软管和气囊组成。
- Remark
- 受托生产企业：广东普门生物医疗科技有限公司；统一社会信用代码：91441900MA4UHLWH4C。
- Appendix
- 产品技术要求
Access comprehensive regulatory information for Intermittent pulse pressure antithrombotic system in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 粤械注准20242090830 and owned by Shenzhen Lifotronic Technology Co., Ltd.. The device was approved on June 25, 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.