Taiwan FDA registration 1320e36edde9d428a2bda84519d5d171
“RET” Intraocular Lens Guide (Sterile)
TW: “瑞特” 人工水晶體導引器 (滅菌)
Taiwan·Risk Class 1·MD·R.E.T., INC.·Registered Mar 05, 2018 – Mar 05, 2023ExpiredRegistration details
- Analysis ID
- 1320e36edde9d428a2bda84519d5d171
- License Form
- Ministry of Health Medical Device Import No. 018859
- Customs Code
- DHA09401885906
Company information
- Manufacturer
- R.E.T., INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4300 Intraocular Lens Guide
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 05, 2018
- Expiry Date
- Mar 05, 2023
About this record
Access comprehensive regulatory information for “RET” Intraocular Lens Guide (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1320e36edde9d428a2bda84519d5d171 and manufactured by R.E.T., INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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