“Thaixon” Guidewire - Taiwan Registration 24b12dd994ab27cb912cb5ad9c885e08
Access comprehensive regulatory information for “Thaixon” Guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 24b12dd994ab27cb912cb5ad9c885e08 and manufactured by GLOBAL-THAIXON PRECISION INDUSTRY CO., LTD. The authorized representative in Taiwan is CHINA SPRING TRADING 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.
Device Details
Registration Details
24b12dd994ab27cb912cb5ad9c885e08
Ministry of Health Medical Device Import No. 029699
DHA05602969901
Product Details
For details Chinese change in the effectiveness of the approved copy of the imitation order: for details, as in the Chinese copy of the imitation approved copy (the original approved copy of the imitation label on May 25, 106 was withdrawn and invalidated).
E Cardiovascular devices
E1330 Catheter Lead
Imported from abroad
Dates and Status
May 11, 2017
May 11, 2027