Pure Global

"Xinghui" Wangdi Double Action Weisting Liquid - Taiwan Registration 9dd5b0c88c52668e4b1ebd8dc90ff6e3

Access comprehensive regulatory information for "Xinghui" Wangdi Double Action Weisting Liquid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9dd5b0c88c52668e4b1ebd8dc90ff6e3 and manufactured by SINPHAR PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is SINPHAR PHARMACEUTICAL 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 Database
Powered by Pure Global AI
89,000+ Devices
9dd5b0c88c52668e4b1ebd8dc90ff6e3
Registration Details
Taiwan FDA Registration: 9dd5b0c88c52668e4b1ebd8dc90ff6e3
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Xinghui" Wangdi Double Action Weisting Liquid
TW: โ€œๆ่ผโ€ๆ—บๆปด้›™ๆ•ˆๆฟ•ๆฝคๆถฒ
Risk Class 2
Cancelled

Registration Details

9dd5b0c88c52668e4b1ebd8dc90ff6e3

DHY00500288506

Company Information

Taiwan, Province of China

Product Details

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

M Ophthalmology

M.5928 Products for the preservation of soft contact lenses

Domestic

Dates and Status

Feb 08, 2010

Dec 31, 2014

Nov 17, 2016

Cancellation Information

Logged out

่‡ช่ซ‹่จป้Šท