Taiwan FDA registration 5fedb129b93056aad5be821305aad2be
Reinter IOL guide (sterilization)
TW: "瑞英特" 人工水晶體導引器(滅菌)
Taiwan·Risk Class 1·RET, INC.·Registered Nov 17, 2022 – Nov 17, 2027ActiveRegistration details
- Analysis ID
- 5fedb129b93056aad5be821305aad2be
- Customs Code
- DHA09402295902
Company information
- Manufacturer
- RET, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CRYSTALVISION 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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Nov 17, 2022
- Expiry Date
- Nov 17, 2027
About this record
Access comprehensive regulatory information for Reinter IOL 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 5fedb129b93056aad5be821305aad2be and manufactured by RET, INC.. The authorized representative in Taiwan is CRYSTALVISION CO., LTD..
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