Taiwan FDA registration 96e7a7b8a7492ef2ed6330df51ab0a84
Pegavision Anti Blue Light Daily Disposable Soft Contact Lenses
TW: 晶碩抗藍光日拋軟性隱形眼鏡
Taiwan·Risk Class 2·MD·PEGAVISION CORPORATION·Registered Apr 15, 2023 – Apr 15, 2028ActiveRegistration details
- Analysis ID
- 96e7a7b8a7492ef2ed6330df51ab0a84
- License Form
- Ministry of Health Medical Device Manufacturing No. 007843
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
- Apr 15, 2023
- Expiry Date
- Apr 15, 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 96e7a7b8a7492ef2ed6330df51ab0a84 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.
Free DatabasePowered by Pure Global AI89,000+ Devices