Taiwan FDA registration 80afcf71a9fc86322e1ba13ae8543725
"Dr. Len" Ruilin Dual Action Wetting Solution
TW: “博士倫”瑞霖雙效潤濕液
Taiwan·Risk Class 2·Bausch & Lomb Incorporated·Registered Oct 22, 2010 – Oct 22, 2025ExpiredRegistration details
- Analysis ID
- 80afcf71a9fc86322e1ba13ae8543725
- Customs Code
- DHA00602160103
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.5928 Products for the preservation of soft contact lenses
- Import Information
- import
Dates and status
- Registration Date
- Oct 22, 2010
- Expiry Date
- Oct 22, 2025
About this record
Access comprehensive regulatory information for "Dr. Len" Ruilin Dual Action Wetting Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80afcf71a9fc86322e1ba13ae8543725 and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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