Taiwan FDA registration 11535b0fd7cdd223207a1ee93b84d184

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·The second factory of Wangfalcon Technology Co., Ltd·Registered May 24, 2021 – May 24, 2026Expired
Registration details
Analysis ID
11535b0fd7cdd223207a1ee93b84d184
License Form
Ministry of Health Medical Device Manufacturing No. 007137
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
VIZIONFOCUS INC.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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
May 24, 2021
Expiry Date
May 24, 2026
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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 11535b0fd7cdd223207a1ee93b84d184 and manufactured by The second factory of Wangfalcon Technology Co., Ltd. The authorized representative in Taiwan is VIZIONFOCUS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VIZIONFOCUS INC., 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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