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"Taiwu" tracheobronchial stent - Taiwan Registration 063071ad3ab8331b335a5fa8a8c0ec4e

Access comprehensive regulatory information for "Taiwu" tracheobronchial stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 063071ad3ab8331b335a5fa8a8c0ec4e and manufactured by TAEWOONG MEDICAL CO., LTD.. The authorized representative in Taiwan is HOPE SING MEDICAL INSTRUMENTS 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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063071ad3ab8331b335a5fa8a8c0ec4e
Registration Details
Taiwan FDA Registration: 063071ad3ab8331b335a5fa8a8c0ec4e
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Device Details

"Taiwu" tracheobronchial stent
TW: โ€œๆณฐๆ‚Ÿโ€ๆฐฃ็ฎกๆ”ฏๆฐฃ็ฎกๆ”ฏๆžถ
Risk Class 2

Registration Details

063071ad3ab8331b335a5fa8a8c0ec4e

DHA00602404106

Company Information

Korea, Republic of

Product Details

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

I General, Plastic Surgery and Dermatology

I.3720 Gas Pipe Supplements

import

Dates and Status

Sep 21, 2012

Sep 21, 2027