Taiwan FDA registration 24b12dd994ab27cb912cb5ad9c885e08

“Thaixon” Guidewire

TW: “泰尚”導引線

Taiwan·Risk Class 2·MD·GLOBAL-THAIXON PRECISION INDUSTRY CO., LTD·Registered May 11, 2017 – May 11, 2027Active

Registration details

Analysis ID: 24b12dd994ab27cb912cb5ad9c885e08
License Form: Ministry of Health Medical Device Import No. 029699
Customs Code: DHA05602969901

Company information

Manufacturer: GLOBAL-THAIXON PRECISION INDUSTRY CO., LTD
Manufacturer Country: Thailand
Authorized Representative: CHINA SPRING TRADING CO., LTD.

Product details

Intended Use: 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the Chinese copy of the imitation approved copy (the original approved copy of the imitation label on May 25, 106 was withdrawn and invalidated).
Product Type (Level 1): E Cardiovascular devices
Product Type (Level 2): E1330 Catheter Lead
Import Information: Imported from abroad

Dates and status

Registration Date: May 11, 2017
Expiry Date: May 11, 2027

About this record

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..

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