Taiwan FDA registration afd64a897051f68286ef9df28d7ba60e

X'ion Corrective Spectacle Lens (Non-Sterile)

TW: 禮昂 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·POLYCORE OPTICAL (HONG KONG) LIMITED·Registered Dec 01, 2016 – Dec 01, 2021Expired
Registration details
Analysis ID
afd64a897051f68286ef9df28d7ba60e
License Form
Ministry of Health Medical Device Import No. 017239
Customs Code
DHA09401723900
Company information
Manufacturer Country
Hong Kong
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
Dec 01, 2016
Expiry Date
Dec 01, 2021
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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 afd64a897051f68286ef9df28d7ba60e and manufactured by POLYCORE OPTICAL (HONG KONG) LIMITED. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 4 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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