Taiwan FDA registration 776eb0ec8ee8ed7a6c4ab7cd34f4e664

GIA Corrective Spectacle Lens (Non-Sterile)

TW: 白鑽矯正鏡片(未滅菌)

Taiwan·Risk Class 1·MD·The third factory of Poly Optical Technology Co., Ltd·Registered Oct 06, 2021 – Oct 06, 2026Active

Registration details

Analysis ID: 776eb0ec8ee8ed7a6c4ab7cd34f4e664
License Form: Ministry of Health Medical Device Manufacturing No. 009342

Company information

Manufacturer: The third factory of Poly Optical Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: POLYLITE TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M5844 corrective lenses
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 06, 2021
Expiry Date: Oct 06, 2026

About this record

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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