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Anyoshi Eye Hydrogel Daily Discarded Contact Lenses - Taiwan Registration c9e36da56637227fdea0f1bb4bc6fe06

Access comprehensive regulatory information for Anyoshi Eye Hydrogel Daily Discarded 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 c9e36da56637227fdea0f1bb4bc6fe06 and manufactured by Johnson & Johnson Vision Care Ireland UC;; Johnson & Johnson Vision Care, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON TAIWAN 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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c9e36da56637227fdea0f1bb4bc6fe06
Registration Details
Taiwan FDA Registration: c9e36da56637227fdea0f1bb4bc6fe06
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Device Details

Anyoshi Eye Hydrogel Daily Discarded Contact Lenses
TW: ๅฎ‰่ฆ–ๅ„ช็›ๆผพๆฐดๅ‡ๆฏๆ—ฅๆ‹‹ๆฃ„ๅผ้šฑๅฝข็œผ้ก
Risk Class 2

Registration Details

c9e36da56637227fdea0f1bb4bc6fe06

DHA05603504709

Company Information

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.5925 ่ปŸๅผ้šฑๅฝข็œผ้ก

import

Dates and Status

Dec 03, 2021

Dec 03, 2026