"Luci" intraocular lens guide (sterilized) - Taiwan Registration 72305620d3a7e4f4a2e92a5f2770734c
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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Device Details
Registration Details
72305620d3a7e4f4a2e92a5f2770734c
DHA09401689908
Product Details
Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
M Ophthalmology
M.4300 Artificial crystal body inducer
Input;; QMS/QSD
Dates and Status
Aug 15, 2016
Aug 15, 2021
Jul 19, 2023
Cancellation Information
Logged out
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