Taiwan FDA registration 93103f7231ef7881851bd521fd1643b1
"Bausch & Brown" IOL guide (unsterilized)
TW: “博士倫”人工水晶體導引器（未滅菌）
Taiwan·Risk Class 1·BAUSCH & LOMB INC.·Registered Oct 27, 2010 – Oct 27, 2025ExpiredRegistration details
- Analysis ID
- 93103f7231ef7881851bd521fd1643b1
- Customs Code
- DHA04400941706
Company information
- Manufacturer
- BAUSCH & LOMB INC.
- 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
- import
Dates and status
- Registration Date
- Oct 27, 2010
- Expiry Date
- Oct 27, 2025
About this record
Access comprehensive regulatory information for "Bausch & Brown" 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 93103f7231ef7881851bd521fd1643b1 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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