Taiwan FDA registration df91cd85336e8b0922ada514be45f390
"Baxter" infusion tube set
TW: "百特"輸液管組
Taiwan·Risk Class 2·BAXTER HEALTHCARE SA, SINGAPORE BRANCH·Registered Jan 03, 2007 – Jan 03, 2012CancelledRegistration details
- Analysis ID
- df91cd85336e8b0922ada514be45f390
- Customs Code
- DHA00601765409
Company information
- Manufacturer
- BAXTER HEALTHCARE SA, SINGAPORE BRANCH
- Manufacturer Country
- Singapore
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5440 血管內輸液套
- Import Information
- import
Dates and status
- Registration Date
- Jan 03, 2007
- Expiry Date
- Jan 03, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baxter" infusion tube set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df91cd85336e8b0922ada514be45f390 and manufactured by BAXTER HEALTHCARE SA, SINGAPORE BRANCH. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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