Taiwan FDA registration 2a221db67be04f2467c3ae6c22f15253
"Dr. Len" Bolshton Enzyme Protein Removal Cleanser
TW: “博士倫”博視頓酵素除蛋白清潔液
Taiwan·Risk Class 2·Bausch & Lomb Incorporated·Registered Jul 23, 2008 – Jul 23, 2028ActiveRegistration details
- Analysis ID
- 2a221db67be04f2467c3ae6c22f15253
- Customs Code
- DHA00601913100
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
- Jul 23, 2008
- Expiry Date
- Jul 23, 2028
About this record
Access comprehensive regulatory information for "Dr. Len" Bolshton Enzyme Protein Removal Cleanser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a221db67be04f2467c3ae6c22f15253 and manufactured by Bausch & Lomb Incorporated. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices