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"Kangqier" Shi Shi Mark capsules - Taiwan Registration 5bdf91cfb884bba09e0d1df6c1626c59

Access comprehensive regulatory information for "Kangqier" Shi Shi Mark capsules in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5bdf91cfb884bba09e0d1df6c1626c59 and manufactured by KONSYL PHARMACEUTICALS, INC.. The authorized representative in Taiwan is WELL SHIP INDUSTRIAL 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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5bdf91cfb884bba09e0d1df6c1626c59
Registration Details
Taiwan FDA Registration: 5bdf91cfb884bba09e0d1df6c1626c59
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Device Details

"Kangqier" Shi Shi Mark capsules
TW: โ€œๅบท่ณœ็ˆพโ€่ฅฟๆ–ฝ้ฆฌๅ…‹่† ๅ›Š
Risk Class 3
Cancelled

Registration Details

5bdf91cfb884bba09e0d1df6c1626c59

DHA00601825500

Company Information

United States

Product Details

For details, please refer to the approved version of Chinese copy.

H Gastroenterology and urology

import

Dates and Status

Apr 12, 2007

Apr 12, 2012

Apr 30, 2014

Cancellation Information

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