Taiwan FDA registration eb3a4bc1e448595f7b1a8afcad4cff1d
"Esco" intraocular lens guide (unsterilized)
TW: “愛斯可”人工水晶體導引器（未滅菌）
Taiwan·Risk Class 1·ASICO LLC·Registered Jan 09, 2008 – Jan 09, 2023ExpiredRegistration details
- Analysis ID
- eb3a4bc1e448595f7b1a8afcad4cff1d
- Customs Code
- DHA04400644904
Company information
- Manufacturer
- ASICO 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)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- import
Dates and status
- Registration Date
- Jan 09, 2008
- Expiry Date
- Jan 09, 2023
About this record
Access comprehensive regulatory information for "Esco" intraocular lens guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eb3a4bc1e448595f7b1a8afcad4cff1d and manufactured by ASICO LLC. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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