"Ruita" intraocular lens guide (sterilization)
Taiwan·Risk Class 1·R.E.T., INC.·Registered May 01, 2015 – May 01, 2030Active- Analysis ID
- 13c56421f65126ef180396ac929e7468
- Customs Code
- DHA09401518707
- Manufacturer
- R.E.T., INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SHENG SHIUAN INDUSTRIAL 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
- Input;; QMS/QSD
- Registration Date
- May 01, 2015
- Expiry Date
- May 01, 2030
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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 13c56421f65126ef180396ac929e7468 and manufactured by R.E.T., INC.. The authorized representative in Taiwan is SHENG SHIUAN INDUSTRIAL CO., LTD..
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