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"Dimak" Y-connector - Taiwan Registration 75f1e3b7a01ab64d5a37a31048ec891e

Access comprehensive regulatory information for "Dimak" Y-connector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75f1e3b7a01ab64d5a37a31048ec891e 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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75f1e3b7a01ab64d5a37a31048ec891e
Registration Details
Taiwan FDA Registration: 75f1e3b7a01ab64d5a37a31048ec891e
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Device Details

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

Registration Details

75f1e3b7a01ab64d5a37a31048ec891e

DHA09200127603

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

Chinese goods;; input

Dates and Status

Dec 24, 2021

Dec 24, 2026