Taiwan FDA registration dca34a26481f670781a64650b4fc4021
"Dr. Len" Dawning Ultrasound Emulsifier
TW: “博士倫”曙光超音波乳化儀
Taiwan·Risk Class 2·BAUSCH & LOMB INC.·Registered Mar 18, 2008 – Mar 18, 2028ActiveRegistration details
- Analysis ID
- dca34a26481f670781a64650b4fc4021
- Customs Code
- DHA00601873705
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.4670 Crystal emulsifier
- Import Information
- import
Dates and status
- Registration Date
- Mar 18, 2008
- Expiry Date
- Mar 18, 2028
About this record
Access comprehensive regulatory information for "Dr. Len" Dawning Ultrasound Emulsifier in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dca34a26481f670781a64650b4fc4021 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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