Taiwan FDA registration 397e8e3205453928cbbdc8ecba8fe9e0

"EYEZEN" Corrective spectacle lens (Non-Sterile)

TW: "愛讚" 矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·ESSILOR MANUFACTURING (THAILAND) CO., LTD.·Registered Dec 06, 2016 – Dec 06, 2026Active

Registration details

Analysis ID: 397e8e3205453928cbbdc8ecba8fe9e0
License Form: Ministry of Health Medical Device Import No. 017249
Customs Code: DHA09401724900

Company information

Manufacturer: ESSILOR MANUFACTURING (THAILAND) CO., LTD.
Manufacturer Country: Thailand
Authorized Representative: ESSILOR-POLYLITE TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M5844 corrective lenses
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 06, 2016
Expiry Date: Dec 06, 2026

About this record

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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