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"Shengyoda" through the middle diaphragm duct system - Taiwan Registration 51a29d87ae0aab7a7b1a6a7f7c18eff6

Access comprehensive regulatory information for "Shengyoda" through the middle diaphragm duct system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51a29d87ae0aab7a7b1a6a7f7c18eff6 and manufactured by ST. JUDE MEDICAL. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies 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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51a29d87ae0aab7a7b1a6a7f7c18eff6
Registration Details
Taiwan FDA Registration: 51a29d87ae0aab7a7b1a6a7f7c18eff6
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Device Details

"Shengyoda" through the middle diaphragm duct system
TW: โ€œ่–็Œท้”โ€็ถ“ไธญ่†ˆๅฐŽ็ฎก็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

51a29d87ae0aab7a7b1a6a7f7c18eff6

DHA00601909904

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1340 ๅฐŽ็ฎกๅฐŽๅผ•ๅ™จ;; E.1390 ๅฅ—็ฎก้‡

import

Dates and Status

Jul 09, 2008

Jul 09, 2018

Jul 15, 2022

Cancellation Information

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