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"Fude" tubing fixture (unsterilized) - Taiwan Registration e7f9e0cdaba9593223fcb34a2fc5c722

Access comprehensive regulatory information for "Fude" tubing fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e7f9e0cdaba9593223fcb34a2fc5c722 and manufactured by E. BENSON HOOD LABORATORIES,INC.. The authorized representative in Taiwan is WHOLE WELL 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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e7f9e0cdaba9593223fcb34a2fc5c722
Registration Details
Taiwan FDA Registration: e7f9e0cdaba9593223fcb34a2fc5c722
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Device Details

"Fude" tubing fixture (unsterilized)
TW: โ€œ็ฆๅพทโ€ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e7f9e0cdaba9593223fcb34a2fc5c722

DHA04401229301

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".

D Anesthesiology

D.5770 ๆฐฃ็ฎก็ฎก่ทฏๅ›บๅฎš่ฃ็ฝฎ

import

Dates and Status

Oct 23, 2012

Oct 23, 2017

Dec 13, 2019

Cancellation Information

Logged out

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