Taiwan FDA registration 5df1ab04fbc9aa5602f480add8b2447e
"Bausch & Lomb" diamond-regulated intraocular lens
TW: “博士倫”晶鑽調節式人工水晶體
Taiwan·Risk Class 3·BAUSCH & LOMB INCORPORATED·Registered Sep 02, 2010 – Sep 02, 2020CancelledRegistration details
- Analysis ID
- 5df1ab04fbc9aa5602f480add8b2447e
- Customs Code
- DHA00602142101
Company information
- Manufacturer
- BAUSCH & LOMB INCORPORATED
- 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
- Sep 02, 2010
- Expiry Date
- Sep 02, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Bausch & Lomb" diamond-regulated 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 5df1ab04fbc9aa5602f480add8b2447e and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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