Taiwan FDA registration 3bde2cba99919a6ccf773d313209ce88
"Alcon" intraocular lens guide (sterilization)
TW: “愛爾康”人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·ALCON RESEARCH, LLC·Registered Mar 07, 2008 – Mar 07, 2028ActiveRegistration details
- Analysis ID
- 3bde2cba99919a6ccf773d313209ce88
- Customs Code
- DHA04400656009
Company information
- Manufacturer
- ALCON RESEARCH, LLC
- Manufacturer Country
- United States
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 07, 2008
- Expiry Date
- Mar 07, 2028
About this record
Access comprehensive regulatory information for "Alcon" intraocular lens guide (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3bde2cba99919a6ccf773d313209ce88 and manufactured by ALCON RESEARCH, LLC. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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