Taiwan FDA registration cccacc0f3bf05e300f5981be741f7b79
Pegavision Anti-Blue Light Daily Disposable Soft Contact Lenses
TW: 晶碩抗藍光日拋軟性隱形眼鏡
Registration details
- Analysis ID
- cccacc0f3bf05e300f5981be741f7b79
- License Form
- Ministry of Health Medical Device Manufacturing No. 007952
Company information
- Manufacturer
- PEGAVISION CORPORATION
- 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
- Jul 17, 2023
- Expiry Date
- Jul 17, 2028
About this record
Access comprehensive regulatory information for Pegavision 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 cccacc0f3bf05e300f5981be741f7b79 and manufactured by PEGAVISION CORPORATION. The authorized representative in Taiwan is PEGAVISION CORPORATION.
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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