Taiwan FDA registration 72305620d3a7e4f4a2e92a5f2770734c
"Luci" intraocular lens guide (sterilized)
TW: "露喜" 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·LUCID KOREA CO., LTD·Registered Aug 15, 2016 – Aug 15, 2021CancelledRegistration details
- Analysis ID
- 72305620d3a7e4f4a2e92a5f2770734c
- Customs Code
- DHA09401689908
Company information
- Manufacturer
- LUCID KOREA CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
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
- Aug 15, 2016
- Expiry Date
- Aug 15, 2021
- Cancellation Date
- Jul 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Luci" intraocular lens guide (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 72305620d3a7e4f4a2e92a5f2770734c and manufactured by LUCID KOREA CO., LTD. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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