Taiwan FDA registration 8b46c3ac329f8a8d3962f6579ff8b951
"Dr. Len" intraocular lens eyeball
TW: "博士倫"人工水晶體眼球
Taiwan·Risk Class 2·BAUSCH & LOMB INC.·Registered May 27, 1999 – Feb 09, 2019CancelledRegistration details
- Analysis ID
- 8b46c3ac329f8a8d3962f6579ff8b951
- Customs Code
- DHA00600917208
Company information
- Manufacturer
- BAUSCH & LOMB INC.
- Manufacturer Country
- United States
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Product Type (Level 1)
- 0314 Intraocular lens
- Import Information
- import
Dates and status
- Registration Date
- May 27, 1999
- Expiry Date
- Feb 09, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Dr. Len" intraocular lens eyeball in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8b46c3ac329f8a8d3962f6579ff8b951 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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