Taiwan FDA registration fb9b8cfcd67647a7c1b1ea4014a7f827

Daily Disposable Silicone Hydrogel Contact Lens Aqualux Series

TW: 涵氧水原力矽水膠日拋隱形眼鏡
Taiwan flagTaiwan·Risk Class 2·MD·HOPE VISION CO., LTD.·Registered Jul 23, 2021 – Mar 12, 2024Expired
Registration details
Analysis ID
fb9b8cfcd67647a7c1b1ea4014a7f827
License Form
Ministry of Health Medical Device Manufacturing No. 007220
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
HOPE VISION CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5925 Flexible Contact Lens
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Jul 23, 2021
Expiry Date
Mar 12, 2024
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About this record

Access comprehensive regulatory information for Daily Disposable Silicone Hydrogel Contact Lens Aqualux Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb9b8cfcd67647a7c1b1ea4014a7f827 and manufactured by HOPE VISION CO., LTD.. The authorized representative in Taiwan is HOPE VISION CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including APEXLENS CO., LTD., and 1 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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