Taiwan FDA registration 7bf753ac8cf5e51ed1d70bf872591aee
Fushi contact lens wetter
TW: 福視美隱形眼鏡濕潤劑
Taiwan·Risk Class 2·TRB CHEMEDICA AG·Registered Aug 27, 2007 – Aug 27, 2022CancelledRegistration details
- Analysis ID
- 7bf753ac8cf5e51ed1d70bf872591aee
- Customs Code
- DHA00601822007
Company information
- Manufacturer
- TRB CHEMEDICA AG
- Manufacturer Country
- Germany
- Authorized Representative
- CENTAPHARM HEALTHCARE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.5928 Products for the preservation of soft contact lenses
- Import Information
- import
Dates and status
- Registration Date
- Aug 27, 2007
- Expiry Date
- Aug 27, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fushi contact lens wetter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7bf753ac8cf5e51ed1d70bf872591aee and manufactured by TRB CHEMEDICA AG. The authorized representative in Taiwan is CENTAPHARM HEALTHCARE 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