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GIA Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 776eb0ec8ee8ed7a6c4ab7cd34f4e664

Access comprehensive regulatory information for GIA 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 776eb0ec8ee8ed7a6c4ab7cd34f4e664 and manufactured by The third factory of Poly Optical Technology Co., Ltd. The authorized representative in Taiwan is POLYLITE TAIWAN CO., LTD..

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776eb0ec8ee8ed7a6c4ab7cd34f4e664
Registration Details
Taiwan FDA Registration: 776eb0ec8ee8ed7a6c4ab7cd34f4e664
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Device Details

GIA Corrective Spectacle Lens (Non-Sterile)
TW: ็™ฝ้‘ฝ ็Ÿฏๆญฃ้ก็‰‡(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

776eb0ec8ee8ed7a6c4ab7cd34f4e664

Ministry of Health Medical Device Manufacturing No. 009342

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.

M Ophthalmic devices

M5844 corrective lenses

Produced in Taiwan, China

Dates and Status

Oct 06, 2021

Oct 06, 2026