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Aurora 1-Day Anti-UV Disposable Contact Lens - Taiwan Registration 43277d6f64a61760a55adf12b121322b

Access comprehensive regulatory information for Aurora 1-Day Anti-UV Disposable 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 43277d6f64a61760a55adf12b121322b and manufactured by I-SEE VISION TECHNOLOGY INC.. The authorized representative in Taiwan is I-SEE VISION TECHNOLOGY INC..

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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43277d6f64a61760a55adf12b121322b
Registration Details
Taiwan FDA Registration: 43277d6f64a61760a55adf12b121322b
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Device Details

Aurora 1-Day Anti-UV Disposable Contact Lens
TW: ๆญ่‹ฅๆ‹‰ๆทจ้€ๆฝคๆŠ—็ดซๅค–็ทšๆ—ฅๆ‹‹้šฑๅฝข็œผ้ก
Risk Class 2
MD

Registration Details

43277d6f64a61760a55adf12b121322b

Ministry of Health Medical Device Manufacturing No. 007027

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M5925 Flexible Contact Lens

Produced in Taiwan, China

Dates and Status

Feb 18, 2021

Apr 30, 2025