Taiwan FDA registration c11c437d463b8f82473af2bb2f0dda81
SharpVision IOL guide (unsterilized)
TW: “銳視特”人工水晶體導引器 (未滅菌)
Taiwan·Risk Class 1·R.E.T. INC.·Registered Oct 07, 2010 – Oct 07, 2025ExpiredRegistration details
- Analysis ID
- c11c437d463b8f82473af2bb2f0dda81
- Customs Code
- DHA04400932501
Company information
- Manufacturer
- R.E.T. INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SHIN SHENG PHARMACEUTICAL CO., LTD.
Product details
- 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
- import
Dates and status
- Registration Date
- Oct 07, 2010
- Expiry Date
- Oct 07, 2025
About this record
Access comprehensive regulatory information for SharpVision IOL guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c11c437d463b8f82473af2bb2f0dda81 and manufactured by R.E.T. INC.. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..
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