Taiwan FDA registration 567606170f424f64e908f8007bf4ec88

S.F. Corrective Spectacle Lens(Non-sterile)

TW: 視優適 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ESSILOR MANUFACTURING (THAILAND) CO., LTD.·Registered Sep 19, 2019 – Sep 19, 2024Expired
Registration details
Analysis ID
567606170f424f64e908f8007bf4ec88
License Form
Ministry of Health Medical Device Import No. 020877
Customs Code
DHA09402087700
Company information
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
Sep 19, 2019
Expiry Date
Sep 19, 2024
About this record

Access comprehensive regulatory information for S.F. 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 567606170f424f64e908f8007bf4ec88 and manufactured by ESSILOR MANUFACTURING (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.

Free DatabasePowered by Pure Global AI89,000+ Devices