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“STELLEST” Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 102583b3c1b1a6f744782256e37680f5

Access comprehensive regulatory information for “STELLEST” 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 102583b3c1b1a6f744782256e37680f5 and manufactured by ESSILOR OPTICAL LABORATORY (THAILAND) CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN 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.

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102583b3c1b1a6f744782256e37680f5
Registration Details
Taiwan FDA Registration: 102583b3c1b1a6f744782256e37680f5
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Device Details

“STELLEST” Corrective Spectacle Lens (Non-Sterile)
TW: “星趣控” 矯正鏡片(未滅菌)
Risk Class 1
MD

Registration Details

102583b3c1b1a6f744782256e37680f5

Ministry of Health Medical Device Import No. 022744

DHA09402274404

Company Information

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 Ophthalmology

M5844 corrective lenses

Imported from abroad

Dates and Status

Feb 14, 2022

Feb 14, 2027