Taiwan FDA registration 102583b3c1b1a6f744782256e37680f5

“STELLEST” Corrective Spectacle Lens (Non-Sterile)

TW: “星趣控” 矯正鏡片(未滅菌)

Taiwan·Risk Class 1·MD·ESSILOR OPTICAL LABORATORY (THAILAND) CO., LTD.·Registered Feb 14, 2022 – Feb 14, 2027Active

Registration details

Analysis ID: 102583b3c1b1a6f744782256e37680f5
License Form: Ministry of Health Medical Device Import No. 022744
Customs Code: DHA09402274404

Company information

Manufacturer: ESSILOR OPTICAL LABORATORY (THAILAND) CO., LTD.
Manufacturer Country: Thailand
Authorized Representative: ESSILOR-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 Ophthalmology
Product Type (Level 2): M5844 corrective lenses
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 14, 2022
Expiry Date: Feb 14, 2027

About this record

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..

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