Taiwan FDA registration f183f7bfcda51eb0df386e43359d7d0b
Rehm IOL guide (unsterilized)
TW: “銳德”人工水晶體導引器（未滅菌）
Taiwan·Risk Class 1·R.E.T. INC.·Registered Feb 10, 2012 – Feb 10, 2017CancelledRegistration details
- Analysis ID
- f183f7bfcda51eb0df386e43359d7d0b
- Customs Code
- DHA04401136301
Company information
- Manufacturer
- R.E.T. INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- UNITED MEDICAL INC.
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 Ophthalmology
- Product Type (Level 2)
- M.4300 Artificial crystal body inducer
- Import Information
- import
Dates and status
- Registration Date
- Feb 10, 2012
- Expiry Date
- Feb 10, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Rehm 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 f183f7bfcda51eb0df386e43359d7d0b and manufactured by R.E.T. INC.. The authorized representative in Taiwan is UNITED MEDICAL INC..
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