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Single-use endotracheal intubation - NMPA Registration 粤械注准20242081570

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.

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Class II
粤械注准20242081570
Single-use endotracheal intubation
一次性使用气管插管
NMPA Registration Number: 粤械注准20242081570
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Intended Use
English

It is used to establish an artificial airway during clinical anesthesia or first aid.

中文

供临床麻醉或急救时建立人工气道用。

Device Classification
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 Information
Registration Number
粤械注准20242081570
Approval Date
November 25, 2024
Expiry Date
November 24, 2029
Registrant
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 Facility
Production Address
广州市番禺区化龙镇国贸大道南45号、47号
Structure and Composition
English

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.

中文

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。

Additional Information
Appendix
产品技术要求