Taiwan FDA registration 28a7948d25e3a6b5245385c6982e66b3
"Bausch & Len" Anshi Subbalanced Saline Solution (Sterilized)
TW: "博士倫"安視亞平衡鹽溶液 （滅菌）
Taiwan·Risk Class 1·BAUSCH & LOMB IRELAND·Registered Oct 27, 2005 – Oct 27, 2010CancelledRegistration details
- Analysis ID
- 28a7948d25e3a6b5245385c6982e66b3
- Customs Code
- DHA04400126903
Company information
- Manufacturer
- BAUSCH & LOMB IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
Product details
- Intended Use
- Physiological food for the eye water.
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2005
- Expiry Date
- Oct 27, 2010
- Cancellation Date
- Nov 01, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bausch & Len" Anshi Subbalanced Saline Solution (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 28a7948d25e3a6b5245385c6982e66b3 and manufactured by BAUSCH & LOMB IRELAND. 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