Taiwan FDA registration 2a73c33effe56d5d1f6a7c94021c39f3

X'ion Corrective Spectacle Lens (Non-Sterile)

TW: 禮昂 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·INTEGRATED LENS TECHNOLOGY PTE LTD·Registered Aug 15, 2016 – Aug 15, 2026Active
Registration details
Analysis ID
2a73c33effe56d5d1f6a7c94021c39f3
License Form
Ministry of Health Medical Device Import No. 016898
Customs Code
DHA09401689806
Company information
Manufacturer Country
Singapore
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
Aug 15, 2016
Expiry Date
Aug 15, 2026
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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 2a73c33effe56d5d1f6a7c94021c39f3 and manufactured by INTEGRATED LENS TECHNOLOGY PTE 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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