Taiwan FDA registration 9a190fa0a406fcabf76778975b942424
"Zunwang" medium frequency pulse therapy instrument
TW: "尊王" 中頻脈衝治療儀
Taiwan·T.Y. SHERRY INTERNATIONAL CO., LTD.·Registered Dec 07, 2004 – May 27, 2014CancelledRegistration details
- Analysis ID
- 9a190fa0a406fcabf76778975b942424
- Customs Code
- DHY00500120900
Company information
- Manufacturer
- T.Y. SHERRY INTERNATIONAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- T.Y. SHERRY INTERNATIONAL CO., LTD.
Product details
- Product Type (Level 1)
- K Neuroscience
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 07, 2004
- Expiry Date
- May 27, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Zunwang" medium frequency pulse therapy instrument in Taiwan's medical device market through Pure Global AI's free database. is registered under number 9a190fa0a406fcabf76778975b942424 and manufactured by T.Y. SHERRY INTERNATIONAL CO., LTD.. The authorized representative in Taiwan is T.Y. SHERRY INTERNATIONAL 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.
Free DatabasePowered by Pure Global AI89,000+ Devices