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“BIOTEQ”Extension Set - Taiwan Registration c9c68314e56fa7d688b7e91aeb32c524

Access comprehensive regulatory information for “BIOTEQ”Extension Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9c68314e56fa7d688b7e91aeb32c524 and manufactured by Bonte Biotechnology Co., Ltd. Yilan Plant 2. The authorized representative in Taiwan is BIOTEQUE CORPORATION.

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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c9c68314e56fa7d688b7e91aeb32c524
Registration Details
Taiwan FDA Registration: c9c68314e56fa7d688b7e91aeb32c524
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Device Details

“BIOTEQ”Extension Set
TW: “邦特”輸液延長管
Risk Class 2
MD

Registration Details

c9c68314e56fa7d688b7e91aeb32c524

Ministry of Health Medical Device Manufacturing No. 007663

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

J General hospital and personal use equipment

J5440 Intravascular infusion sleeve

Produced in Taiwan, China

Dates and Status

Jul 24, 2022

Jul 24, 2027