"Ruita" intraocular lens guide (sterilization)
Taiwan·Risk Class 1·RET, INC.·Registered Jul 18, 2022 – Jul 18, 2027Active- Analysis ID
- fc61334475bbcb96866d8e6893f73ddc
- Customs Code
- DHA09402285105
- Manufacturer
- RET, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- IKI MEDICAL CO., LTD.
- 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
- Registration Date
- Jul 18, 2022
- Expiry Date
- Jul 18, 2027
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Access comprehensive regulatory information for "Ruita" 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 fc61334475bbcb96866d8e6893f73ddc and manufactured by RET, INC.. The authorized representative in Taiwan is IKI MEDICAL CO., LTD..
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