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Aurora 1 day blue light block contact lens - Taiwan Registration 8ef70289cd5806e5136c044ebbb3f6f1

Access comprehensive regulatory information for Aurora 1 day blue light block contact lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8ef70289cd5806e5136c044ebbb3f6f1 and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is VIZIONFOCUS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including The second factory of Wangfalcon Technology 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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8ef70289cd5806e5136c044ebbb3f6f1
Registration Details
Taiwan FDA Registration: 8ef70289cd5806e5136c044ebbb3f6f1
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Device Details

Aurora 1 day blue light block contact lens
TW: ๆฅตๅ…‰ๆ—ฅๆ‹‹ๆฟพ่—ๅ…‰้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

8ef70289cd5806e5136c044ebbb3f6f1

Ministry of Health Medical Device Manufacturing No. 007001

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M5925 Flexible Contact Lens

Produced in Taiwan, China

Dates and Status

Dec 28, 2020

Dec 28, 2025

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