Taiwan FDA registration 957aa666f44bff6d1a9dbd0031be66a1

AQUAMAX Anti Blue Light Daily Disposable Soft Contact Lenses

TW: 水滋氧日拋軟性隱形眼鏡(可過濾部份藍光)
Taiwan flagTaiwan·Risk Class 2·MD·PEGAVISION CORPORATION·Registered Jun 17, 2023 – Jun 17, 2028Active
Registration details
Analysis ID
957aa666f44bff6d1a9dbd0031be66a1
License Form
Ministry of Health Medical Device Manufacturing No. 007936
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
PEGAVISION CORPORATION
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M5925 Flexible Contact Lens
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Jun 17, 2023
Expiry Date
Jun 17, 2028
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About this record

Access comprehensive regulatory information for AQUAMAX Anti Blue Light Daily Disposable Soft Contact Lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 957aa666f44bff6d1a9dbd0031be66a1 and manufactured by PEGAVISION CORPORATION. The authorized representative in Taiwan is PEGAVISION CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PEGAVISION CORPORATION, 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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