Single-use endotracheal intubation
- Device class
- Class II
- Model specifications
- 7.0mm、7.5mm、8.0mm
- Approval department
- Guangdong Provincial Drug Administration广东省药品监督管理局
- Registration number
- 粤械注准20242081570
- Approval date
- November 25, 2024
- Expiry date
- November 24, 2029
- Name
- Well Lead Medical Co., Ltd.广州维力医疗器械股份有限公司
- Province/Region
- Guangdong广东
- Address
- No. 4, Area C, Jinhu Industrial City, Hualong Town, Panyu District, Guangzhou广州市番禺区化龙镇金湖工业城C区4号
- Production address
- 广州市番禺区化龙镇国贸大道南45号、47号
It is used to establish an artificial airway during clinical anesthesia or first aid.
供临床麻醉或急救时建立人工气道用。
一次性使用气管插管主要由吸引管、平衡压力/冲洗/CO2样本采集管、套囊充/放气管、主管、套囊、接头和墨菲孔组成.产品经环氧乙烷灭菌,无菌提供,一次性使用.
一次性使用气管插管主要由吸引管、平衡压力/冲洗/CO2样本采集管、套囊充/放气管、主管、套囊、接头和墨菲孔组成。产品经环氧乙烷灭菌，无菌提供，一次性使用。
- Appendix
- 产品技术要求
Access comprehensive regulatory information for Single-use endotracheal intubation 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20242081570 and owned by Well Lead Medical Co., Ltd.. The device was approved on November 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.