Taiwan FDA registration ff37caed2055a3993e5b758814c8815c
Vivid Ophthalmic viscoelastic agent
TW: 維視愛眼科黏彈劑
Taiwan·Risk Class 3·MAXIGEN BIOTECH INC.·Registered Dec 23, 2020 – Feb 04, 2030ActiveRegistration details
- Analysis ID
- ff37caed2055a3993e5b758814c8815c
- Customs Code
- DHY00500126204
Company information
- Manufacturer
- MAXIGEN BIOTECH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MAXIGEN BIOTECH INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 23, 2020
- Expiry Date
- Feb 04, 2030
About this record
Access comprehensive regulatory information for Vivid Ophthalmic viscoelastic agent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ff37caed2055a3993e5b758814c8815c and manufactured by MAXIGEN BIOTECH INC.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..
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