X'ion Corrective Spectacle Lens (Non-Sterile)
Taiwan·Risk Class 1·MD·ESSILOR OF AMERICA, INC.·Registered Sep 08, 2016 – Sep 08, 2026Active- Analysis ID
- bebdc2b4ede5ae99619831706804f297
- License Form
- Ministry of Health Medical Device Import No. 016979
- Customs Code
- DHA09401697906
- Manufacturer
- ESSILOR OF AMERICA, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ESSILOR-POLYLITE TAIWAN CO., LTD.
- 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
- Registration Date
- Sep 08, 2016
- Expiry Date
- Sep 08, 2026
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Access comprehensive regulatory information for X'ion 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 bebdc2b4ede5ae99619831706804f297 and manufactured by ESSILOR OF AMERICA, INC.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including POLYCORE OPTICAL (HONG KONG) LIMITED, INTEGRATED LENS TECHNOLOGY PTE LTD, and 4 recent registrations in the same category. 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.