Taiwan FDA registration 24b68d5f4249801ee6cd46a8880a710f
"Baide" Fenwal plasma pressure plate (unsterilized)
TW: “佰德”芬沃血漿壓板 (未滅菌)
Taiwan·Risk Class 1·BAXTER HEALTHCARE CORPORATION·Registered Aug 20, 2009 – Aug 20, 2014CancelledRegistration details
- Analysis ID
- 24b68d5f4249801ee6cd46a8880a710f
- Customs Code
- DHA04400797300
Company information
- Manufacturer
- BAXTER HEALTHCARE CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Y.H. BIOTEK CO., LTD.
Product details
- Intended Use
- The blood component pressure device can separate various blood components from the whole blood after centrifugation, and does not contain sensors and weighing devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9050 Blood bank supply equipment
- Import Information
- import
Dates and status
- Registration Date
- Aug 20, 2009
- Expiry Date
- Aug 20, 2014
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baide" Fenwal plasma pressure plate (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 24b68d5f4249801ee6cd46a8880a710f and manufactured by BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..
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