Taiwan FDA registration 36ba558c73266279b0a873c880131e67
"Dr. Len" posterior chamber vitrectomy surgical kit
TW: “博士倫”後房玻璃體切除手術包
Taiwan·Risk Class 2·BAUSCH & LOMB INCORPORATED·Registered May 15, 2009 – May 15, 2019CancelledRegistration details
- Analysis ID
- 36ba558c73266279b0a873c880131e67
- Customs Code
- DHA00601985503
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.4150 Vitreous Suction and Cutting Apparatus
- Import Information
- import
Dates and status
- Registration Date
- May 15, 2009
- Expiry Date
- May 15, 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" posterior chamber vitrectomy surgical kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36ba558c73266279b0a873c880131e67 and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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