Pure Global

"EyePro" Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration c41bf6a0d864471102cb7be8120cc958

Access comprehensive regulatory information for "EyePro" Corrective Spectacle Lens (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c41bf6a0d864471102cb7be8120cc958 and manufactured by SUNDEX OPTICAL CO., LTD.. The authorized representative in Taiwan is Chaoqun Optical Glasses 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
c41bf6a0d864471102cb7be8120cc958
Registration Details
Taiwan FDA Registration: c41bf6a0d864471102cb7be8120cc958
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"EyePro" Corrective Spectacle Lens (Non-Sterile)
TW: "ๆ„›้‰‘" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c41bf6a0d864471102cb7be8120cc958

Ministry of Health Medical Device Manufacturing No. 007357

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Jul 19, 2018

Jul 19, 2023