Taiwan FDA registration a3f7d8e562ea2f38a16012c759434bc1

OxyVision Plus Day Flex Contact Lenses

TW: 氧視加日拋軟式隱形眼鏡
Taiwan flagTaiwan·Risk Class 2·VIZIONFOCUS INC.·Registered Aug 31, 2021 – Nov 07, 2027Active
Registration details
Analysis ID
a3f7d8e562ea2f38a16012c759434bc1
Company information
Manufacturer
VIZIONFOCUS INC.
Manufacturer Country
Taiwan, Province of China
Authorized Representative
BRIGHTEN OPTIX CORPORATION
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5925 軟式隱形眼鏡
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Aug 31, 2021
Expiry Date
Nov 07, 2027
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About this record

Access comprehensive regulatory information for OxyVision Plus Day Flex Contact Lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3f7d8e562ea2f38a16012c759434bc1 and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is BRIGHTEN OPTIX CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including The second factory of Wangfalcon Technology Co., Ltd, VIZIONFOCUS INC., and 2 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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