Taiwan FDA registration 8ef70289cd5806e5136c044ebbb3f6f1

Aurora 1 day blue light block contact lens

TW: 極光日拋濾藍光隱形眼鏡
Taiwan flagTaiwan·Risk Class 2·MD·VIZIONFOCUS INC.·Registered Dec 28, 2020 – Dec 28, 2025Expired
Registration details
Analysis ID
8ef70289cd5806e5136c044ebbb3f6f1
License Form
Ministry of Health Medical Device Manufacturing No. 007001
Company information
Manufacturer
VIZIONFOCUS INC.
Manufacturer Country
Taiwan, Province of China
Authorized Representative
VIZIONFOCUS INC.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5925 Flexible Contact Lens
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Dec 28, 2020
Expiry Date
Dec 28, 2025
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About this record

Access comprehensive regulatory information for Aurora 1 day blue light block 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 8ef70289cd5806e5136c044ebbb3f6f1 and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is VIZIONFOCUS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including The second factory of Wangfalcon Technology Co., Ltd, and 1 recent registrations in the same category. 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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