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"Dimak" multi-way connector - Taiwan Registration 888d58f0bbe08b7c6c1d38f9c0775185

Access comprehensive regulatory information for "Dimak" multi-way connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 888d58f0bbe08b7c6c1d38f9c0775185 and manufactured by Beijing Demax Medical Technology Co., Ltd.. The authorized representative in Taiwan is NO.1 BIOTECHNOLOGY 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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888d58f0bbe08b7c6c1d38f9c0775185
Registration Details
Taiwan FDA Registration: 888d58f0bbe08b7c6c1d38f9c0775185
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Device Details

"Dimak" multi-way connector
TW: โ€œ่ฟช็‘ชๅ…‹โ€ ๅคš่ทฏ้€ฃๆŽฅๅ™จ
Risk Class 2

Registration Details

888d58f0bbe08b7c6c1d38f9c0775185

DHA09200127501

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.4290 Arterial vascular bypass surgery with contact pistons, multi-pipe connections or attachments

Input;; Chinese goods

Dates and Status

Dec 24, 2021

Dec 24, 2026