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“TUNGSHI” TRINITY RESUSCITATIR SET - Taiwan Registration 17f0171373498200abba20a9407d87a6

Access comprehensive regulatory information for “TUNGSHI” TRINITY RESUSCITATIR SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17f0171373498200abba20a9407d87a6 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is TUNGSHI MEDICAL EQUIPMENT 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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17f0171373498200abba20a9407d87a6
Registration Details
Taiwan FDA Registration: 17f0171373498200abba20a9407d87a6
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Device Details

“TUNGSHI” TRINITY RESUSCITATIR SET
TW: “銅璽” 三合一甦醒器組
Risk Class 2
MD

Registration Details

17f0171373498200abba20a9407d87a6

Ministry of Health Medical Device Manufacturing No. 004550

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

Mar 24, 2014

Mar 24, 2024