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“Micro-Tech” Tracheal/Bronchial Stent - Taiwan Registration 06584f4471556ba851d5f130de9e324b

Access comprehensive regulatory information for “Micro-Tech” Tracheal/Bronchial Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06584f4471556ba851d5f130de9e324b and manufactured by Micro-Tech (Nanjing) Co., Ltd.. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE 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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06584f4471556ba851d5f130de9e324b
Registration Details
Taiwan FDA Registration: 06584f4471556ba851d5f130de9e324b
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Device Details

“Micro-Tech” Tracheal/Bronchial Stent
TW: “微創”氣管支氣管支架
Risk Class 2
MD

Registration Details

06584f4471556ba851d5f130de9e324b

Ministry of Health Medical Device Land Transport No. 001120

DHA09200112001

Company Information

Product Details

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

I General and plastic surgical devices

I3720 Tracheal Supplement

Imported from abroad; Made in China

Dates and Status

Mar 28, 2020

Mar 28, 2025