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Aquacolor Daily Contact Lens - Taiwan Registration 3015cc64f1bdeaecf6ea60fe1b4876e1

Access comprehensive regulatory information for Aquacolor Daily 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 3015cc64f1bdeaecf6ea60fe1b4876e1 and manufactured by PEGAVISION CORPORATION. The authorized representative in Taiwan is PEGAVISION CORPORATION.

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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3015cc64f1bdeaecf6ea60fe1b4876e1
Registration Details
Taiwan FDA Registration: 3015cc64f1bdeaecf6ea60fe1b4876e1
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Device Details

Aquacolor Daily Contact Lens
TW: ๆฐดๆฝคๆ—ฅๆ‹‹ๅฝฉ็‰‡่ปŸๆ€ง้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

3015cc64f1bdeaecf6ea60fe1b4876e1

Ministry of Health Medical Device Manufacturing No. 007845

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M5925 Flexible Contact Lens

Produced in Taiwan, China

Dates and Status

Apr 09, 2023

Jul 06, 2025