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“Mediair” Trinity Resuscitator Set - Taiwan Registration d5143e093b180225f621da6be6796ec6

Access comprehensive regulatory information for “Mediair” Trinity 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 d5143e093b180225f621da6be6796ec6 and manufactured by Shangyue Technology Co., Ltd. Precision Factory. The authorized representative in Taiwan is EMG 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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d5143e093b180225f621da6be6796ec6
Registration Details
Taiwan FDA Registration: d5143e093b180225f621da6be6796ec6
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Device Details

“Mediair” Trinity Resuscitator Set
TW: “上岳”三合一甦醒器
Risk Class 2
MD

Registration Details

d5143e093b180225f621da6be6796ec6

Ministry of Health Medical Device Manufacturing No. 007245

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

D Devices for anesthesiology

D5925 Powered Emergency Respirator

Produced in Taiwan, China

Dates and Status

Sep 01, 2021

Sep 01, 2026