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AURORA Monthly disposable silicone hydrogel contact lens - Taiwan Registration ab8fa13e1ea676a507f3512dba30ca70

Access comprehensive regulatory information for AURORA Monthly disposable silicone hydrogel 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 ab8fa13e1ea676a507f3512dba30ca70 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. 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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ab8fa13e1ea676a507f3512dba30ca70
Registration Details
Taiwan FDA Registration: ab8fa13e1ea676a507f3512dba30ca70
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Device Details

AURORA Monthly disposable silicone hydrogel contact lens
TW: ๆญ่‹ฅๆ‹‰ๆœˆๆ‹‹็Ÿฝๆฐด่† ้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

ab8fa13e1ea676a507f3512dba30ca70

Ministry of Health Medical Device Manufacturing No. 007204

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmic devices

M5925 Flexible Contact Lens

Produced in Taiwan, China

Dates and Status

Jun 24, 2021

Jul 03, 2025