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"TIDI" Intravascular catheter securement device (Non-Sterile) - Taiwan Registration 9121a12297dfeaf155a939d5997dc9d0

Access comprehensive regulatory information for "TIDI" Intravascular catheter securement device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9121a12297dfeaf155a939d5997dc9d0 and manufactured by TIDI PRODUCTS, LLC. The authorized representative in Taiwan is FRIENDS SCIENTIFIC 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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9121a12297dfeaf155a939d5997dc9d0
Registration Details
Taiwan FDA Registration: 9121a12297dfeaf155a939d5997dc9d0
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Device Details

"TIDI" Intravascular catheter securement device (Non-Sterile)
TW: "่ฟช่‰พ่ฟช่‰พ" ่ก€็ฎกๅ…งๅฐŽ็ฎกๅ›บๅฎš่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9121a12297dfeaf155a939d5997dc9d0

Ministry of Health Medical Device Import No. 018301

DHA09401830107

Company Information

United States

Product Details

Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J5210 Endovascular catheter fixation device

Imported from abroad

Dates and Status

Sep 12, 2017

Sep 12, 2022