Disposable respiratory filter pack - NMPA Registration 豫械注准20202081391
Access comprehensive regulatory information for Disposable respiratory filter pack in the China medical device market through Pure Global AI's free database. This Class II medical device is registered under NMPA registration number 豫械注准20202081391 and owned by Henan Yadu Industrial Co., Ltd.. The device was approved on July 18, 2022.
This page provides complete registration details including registrant information, province location (Henan), 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 suitable for one-time use by medical units as a gas purification and endotracheal intubation auxiliary device for anesthesia machines or ventilators during general anesthesia, postoperative recovery and intensive care.
适用于医疗单位在患者全身麻醉、术后恢复和重症监护时，作为麻醉机或呼吸机的气体净化和气管插管的连接辅助器械一次性使用。
It is composed of basic configuration disposable anesthesia breathing circuit (adult type I/ADULT II/ADULT TYPE III/ADULT TYPE IV/ADULT V / ADULT TYPE VI/PEDIATRIC TYPE I/PEDIATRIC TYPE II/PEDIATRIC TYPE III/PEDIATRIC IV/PEDIATRIC V type/pediatric type VI), disposable heat and moisture exchange filter and optional configuration disposable anesthesia mask.
由基本配置一次性使用麻醉呼吸管路（成人 I型/成人II型/成人III型/成人IV型/成人V型/成人VI型/小儿 I型/小儿II型/小儿III型/小儿IV型/小儿V型/小儿VI型）、一次性使用热湿交换过滤器和选用配置一次性使用麻醉面罩组成。