Taiwan FDA registration 3df1e50bce17de1e68cd3436bd33ed7a
"Bausch & Len" Brighton New Cleansing Multi-functional Solution
TW: “博士倫”博視頓新潔多功能護理液
Taiwan·Risk Class 2·Bausch & Lomb Incorporated·Registered Mar 26, 2009 – Mar 26, 2029ActiveRegistration details
- Analysis ID
- 3df1e50bce17de1e68cd3436bd33ed7a
- Customs Code
- DHA00601973901
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.5918 Rigid Breathable Contact Lens Preservation Products
- Import Information
- import
Dates and status
- Registration Date
- Mar 26, 2009
- Expiry Date
- Mar 26, 2029
About this record
Access comprehensive regulatory information for "Bausch & Len" Brighton New Cleansing Multi-functional Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3df1e50bce17de1e68cd3436bd33ed7a and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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