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"EYEZEN" Corrective spectacle lens (Non-Sterile) - Taiwan Registration 397e8e3205453928cbbdc8ecba8fe9e0

Access comprehensive regulatory information for "EYEZEN" 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 397e8e3205453928cbbdc8ecba8fe9e0 and manufactured by ESSILOR MANUFACTURING (THAILAND) CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

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397e8e3205453928cbbdc8ecba8fe9e0
Registration Details
Taiwan FDA Registration: 397e8e3205453928cbbdc8ecba8fe9e0
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Device Details

"EYEZEN" Corrective spectacle lens (Non-Sterile)
TW: "ๆ„›่ฎš" ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

397e8e3205453928cbbdc8ecba8fe9e0

Ministry of Health Medical Device Import No. 017249

DHA09401724900

Company Information

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

Imported from abroad

Dates and Status

Dec 06, 2016

Dec 06, 2026