Taiwan FDA registration 3015cc64f1bdeaecf6ea60fe1b4876e1
Aquacolor Daily Contact Lens
TW: 水潤日拋彩片軟性隱形眼鏡
Taiwan·Risk Class 2·MD·PEGAVISION CORPORATION·Registered Apr 09, 2023 – Jul 06, 2025ExpiredRegistration details
- Analysis ID
- 3015cc64f1bdeaecf6ea60fe1b4876e1
- License Form
- Ministry of Health Medical Device Manufacturing No. 007845
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 09, 2023
- Expiry Date
- Jul 06, 2025
About this record
Access comprehensive regulatory information for Aquacolor Daily 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 3015cc64f1bdeaecf6ea60fe1b4876e1 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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