Taiwan FDA registration 0e618625ad164e60c29e54488fcd435c
"Bausch & Len" IOL Guides (Sterile/Unsterile)
TW: "博士倫" 人工水晶體導引器(滅菌/未滅菌)
Taiwan·Risk Class 1·Bausch & Lomb Incorporated·Registered Mar 24, 2023 – Mar 24, 2028ActiveRegistration details
- Analysis ID
- 0e618625ad164e60c29e54488fcd435c
- Customs Code
- DHA09402308001
Company information
- Manufacturer
- Bausch & Lomb Incorporated
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 24, 2023
- Expiry Date
- Mar 24, 2028
About this record
Access comprehensive regulatory information for "Bausch & Len" IOL Guides (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e618625ad164e60c29e54488fcd435c and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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