Taiwan FDA registration a9adf110861742edd89449a6bbba5ead
"Alcon" IOL guide (sterilization)
TW: "愛爾康" 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·ALCON RESEARCH, LTD.·Registered Jun 30, 2015 – Jun 30, 2020CancelledRegistration details
- Analysis ID
- a9adf110861742edd89449a6bbba5ead
- Customs Code
- DHA09401539603
Company information
- Manufacturer
- ALCON RESEARCH, LTD.
- 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 30, 2015
- Expiry Date
- Jun 30, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Alcon" IOL 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 a9adf110861742edd89449a6bbba5ead and manufactured by ALCON RESEARCH, LTD.. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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