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“Acare” Demand Valve Resuscitator Set - Taiwan Registration 9b62719c8796da67aee08272559bc55d

Access comprehensive regulatory information for “Acare” Demand Valve Resuscitator Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9b62719c8796da67aee08272559bc55d and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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9b62719c8796da67aee08272559bc55d
Registration Details
Taiwan FDA Registration: 9b62719c8796da67aee08272559bc55d
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Device Details

“Acare” Demand Valve Resuscitator Set
TW: “眾里”三合一甦醒組
Risk Class 2
MD

Registration Details

9b62719c8796da67aee08272559bc55d

Ministry of Health Medical Device Manufacturing No. 004877

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5925 Powered Emergency Respirator

Produced in Taiwan, China

Dates and Status

Dec 23, 2014

Dec 23, 2024