Single-use enhanced endotracheal tube kit - NMPA Registration 粤械注准20232081975
Access comprehensive regulatory information for Single-use enhanced endotracheal tube kit 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20232081975 and owned by Well Lead Medical Co., Ltd.. The device was approved on November 29, 2023.
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.
It is intended for one-time use when the medical department performs endotracheal intubation on patients.
供医疗部门对患者实施气管插管术时一次性使用。
Single-use enhanced endotracheal tube kits include single-use enhanced endotracheal intubation (standard with cuff, standard without cuff, pad with cuff, double balloon, cuff with suction cavity), endotracheal intubation clip (optional), mouthpiece (optional), balloon inflator (optional), suction catheter for respiratory tract (optional), suction tube for suction device, medical rubber gloves, medical absorbent gauze, non-woven fabric (drape), intubation guidewire (optional), bandage (optional), adhesive tape (optional), Oropharyngeal airway (optional) and peephole (optional).
一次性使用加强型气管插管套件包括一次性使用加强型气管插管（标准型带套囊、标准型不带套囊、牙垫型带套囊、双球囊型、带吸痰腔型带套囊）、气管插管固定夹（选配）、咬嘴（选配）、球囊充起器（选配）、呼吸道用吸引导管（选配）、吸引器连接管、医用橡胶手套、医用脱脂纱布、非织造布（铺巾）、插管导丝（选配）、绷带（选配）、胶贴（选配）、口咽通气道（选配）、窥视片（选配）组成。