Taiwan FDA registration ec390517abac22bc00e59f047512046d
Bovine serum albumin solution (unsterilized)
TW: 保脈牛血清白蛋白溶液(未滅菌)
Taiwan·Risk Class 1·CSL LIMITED·Registered Nov 26, 2010 – Nov 26, 2015CancelledRegistration details
- Analysis ID
- ec390517abac22bc00e59f047512046d
- Customs Code
- DHA04400958909
Company information
- Manufacturer
- CSL LIMITED
- Manufacturer Country
- Australia
- Authorized Representative
- GIRAFFES PHARMACEUTICAL COMPANY LTD.
Product details
- Intended Use
- Limited to the first level identification range of intensive medium (B.9600) for in vitro diagnosis of medical device management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9600 Intensive medium for in vitro diagnostics
- Import Information
- import
Dates and status
- Registration Date
- Nov 26, 2010
- Expiry Date
- Nov 26, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Bovine serum albumin solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec390517abac22bc00e59f047512046d and manufactured by CSL LIMITED. The authorized representative in Taiwan is GIRAFFES PHARMACEUTICAL COMPANY LTD..
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