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RêVIA Blue Light Barrier 1 Day Contact Lens - Taiwan Registration 20852079afc21b6129d58e9d7d73c6ca

Access comprehensive regulatory information for RêVIA Blue Light Barrier 1 Day 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 20852079afc21b6129d58e9d7d73c6ca and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is VIZIONFOCUS 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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20852079afc21b6129d58e9d7d73c6ca
Registration Details
Taiwan FDA Registration: 20852079afc21b6129d58e9d7d73c6ca
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Device Details

RêVIA Blue Light Barrier 1 Day Contact Lens
TW: 蕾美濾藍光日拋隱形眼鏡
Risk Class 2
MD

Registration Details

20852079afc21b6129d58e9d7d73c6ca

Ministry of Health Medical Device Manufacturing No. 007104

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

Mar 23, 2021

Dec 28, 2025