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AQUAMAX SUNLIGHT DAILY DISPOSABLE SOFT CONTACT LENSES - Taiwan Registration 9df5925b7afa790f9b7763d59e294b7a

Access comprehensive regulatory information for AQUAMAX SUNLIGHT DAILY DISPOSABLE SOFT 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 9df5925b7afa790f9b7763d59e294b7a 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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9df5925b7afa790f9b7763d59e294b7a
Registration Details
Taiwan FDA Registration: 9df5925b7afa790f9b7763d59e294b7a
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Device Details

AQUAMAX SUNLIGHT DAILY DISPOSABLE SOFT CONTACT LENSES
TW: ๆฐดๆป‹ๆฐง้™ฝๅ…‰ๆ™ถ็ฒนๆ—ฅๆ‹‹่ปŸๆ€ง้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

9df5925b7afa790f9b7763d59e294b7a

Ministry of Health Medical Device Manufacturing No. 007787

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

Dec 24, 2022

Dec 24, 2027