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“Thaixon” Hydrophilic Guidewire - Taiwan Registration cf14b968d99aa0c86643a9b5ddd361e3

Access comprehensive regulatory information for “Thaixon” Hydrophilic Guidewire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cf14b968d99aa0c86643a9b5ddd361e3 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.

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cf14b968d99aa0c86643a9b5ddd361e3
Registration Details
Taiwan FDA Registration: cf14b968d99aa0c86643a9b5ddd361e3
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Device Details

“Thaixon” Hydrophilic Guidewire
TW: “泰尚”親水性鎳鈦合金導引線
Risk Class 2
MD

Registration Details

cf14b968d99aa0c86643a9b5ddd361e3

Ministry of Health Medical Device Import No. 033867

DHA05603386701

Company Information

Product Details

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

E Cardiovascular devices

E1330 Catheter Lead

Imported from abroad

Dates and Status

Jul 29, 2020

Jul 29, 2025