Taiwan FDA registration 5a1a85ca57f6a84afccc840bb422fc9e

X'ion Corrective Spectacle Lens (Non-Sterile)

TW: 禮昂 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·JIANGSU YOULI OPTICS SPECTACLES CO., LTD.·Registered Jul 30, 2015 – Jul 30, 2025Expired
Registration details
Analysis ID
5a1a85ca57f6a84afccc840bb422fc9e
License Form
Ministry of Health Medical Device Land Transport No. 002463
Customs Code
DHA09600246300
Company information
Manufacturer Country
China
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; Made in China
Dates and status
Registration Date
Jul 30, 2015
Expiry Date
Jul 30, 2025
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About this record

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 5a1a85ca57f6a84afccc840bb422fc9e and manufactured by JIANGSU YOULI OPTICS SPECTACLES CO., LTD.. 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, ESSILOR OF AMERICA, INC., 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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