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SEESCAN Daily Disposable Silicone Hydrogel Contact Lens - Taiwan Registration e488c7dc34d41ee7519b046f33904a43

Access comprehensive regulatory information for SEESCAN Daily 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 e488c7dc34d41ee7519b046f33904a43 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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e488c7dc34d41ee7519b046f33904a43
Registration Details
Taiwan FDA Registration: e488c7dc34d41ee7519b046f33904a43
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Device Details

SEESCAN Daily Disposable Silicone Hydrogel Contact Lens
TW: ็Ÿฝ่ฆ–ๅบทๆ—ฅๆ‹‹็Ÿฝๆฐด่† ้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

e488c7dc34d41ee7519b046f33904a43

Ministry of Health Medical Device Manufacturing No. 007318

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

Oct 25, 2021

Mar 12, 2024