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X'ion Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration bebdc2b4ede5ae99619831706804f297

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.

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bebdc2b4ede5ae99619831706804f297
Registration Details
Taiwan FDA Registration: bebdc2b4ede5ae99619831706804f297
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Device Details

X'ion Corrective Spectacle Lens (Non-Sterile)
TW: ็ฆฎๆ˜‚ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

bebdc2b4ede5ae99619831706804f297

Ministry of Health Medical Device Import No. 016979

DHA09401697906

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Sep 08, 2016

Sep 08, 2026