Taiwan FDA registration 5cd3243a4ec0089ca15458971a00fa72
"Dr. Len" Ansipin artificial vitreous
TW: "博士倫" 安視平人工玻璃體
Taiwan·MANUFACTURED BY ANIKA THERAPEUTICS, INC. FOR BAUSCH & LOMB INC.·Registered Dec 23, 2004 – Dec 23, 2009CancelledRegistration details
- Analysis ID
- 5cd3243a4ec0089ca15458971a00fa72
- Customs Code
- DHA00601097201
Company information
- 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
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 23, 2004
- Expiry Date
- Dec 23, 2009
- Cancellation Date
- Jun 30, 2010
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Dr. Len" Ansipin artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. is registered under number 5cd3243a4ec0089ca15458971a00fa72 and manufactured by MANUFACTURED BY ANIKA THERAPEUTICS, INC. FOR BAUSCH & LOMB INC.. 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