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OxyVision Plus Day Flex Contact Lenses - Taiwan Registration a3f7d8e562ea2f38a16012c759434bc1

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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a3f7d8e562ea2f38a16012c759434bc1
Registration Details
Taiwan FDA Registration: a3f7d8e562ea2f38a16012c759434bc1
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Device Details

OxyVision Plus Day Flex Contact Lenses
TW: ๆฐง่ฆ–ๅŠ ๆ—ฅๆ‹‹่ปŸๅผ้šฑๅฝข็œผ้ก
Risk Class 2

Registration Details

a3f7d8e562ea2f38a16012c759434bc1

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.5925 ่ปŸๅผ้šฑๅฝข็œผ้ก

Domestic;; Contract manufacturing

Dates and Status

Aug 31, 2021

Nov 07, 2027

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