Taiwan FDA registration c30406fc5c591a4a5a34bda73cbba5d7
"Bausch & Lomb" Youshi aspheric intraocular lens
TW: “博士倫”優視非球面人工水晶體
Taiwan·Risk Class 3·BAUSCH & LOMB, INC.·Registered Mar 31, 2011 – Mar 31, 2026ExpiredRegistration details
- Analysis ID
- c30406fc5c591a4a5a34bda73cbba5d7
- Customs Code
- DHA00602225502
Company information
- Manufacturer
- BAUSCH & LOMB, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- import
Dates and status
- Registration Date
- Mar 31, 2011
- Expiry Date
- Mar 31, 2026
About this record
Access comprehensive regulatory information for "Bausch & Lomb" Youshi aspheric intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number c30406fc5c591a4a5a34bda73cbba5d7 and manufactured by BAUSCH & LOMB, INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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