Taiwan FDA registration cf3746e1c652b0a61b8b6bffae65bf7c
"Baxter" light-protected intravenous infusion tube set
TW: “百特”避光靜脈輸液管組
Taiwan·Risk Class 2·BAXTER (MALTA) LTD.·Registered Nov 13, 2009 – Nov 13, 2014CancelledRegistration details
- Analysis ID
- cf3746e1c652b0a61b8b6bffae65bf7c
- Customs Code
- DHA00602032003
Company information
- Manufacturer
- BAXTER (MALTA) LTD.
- Manufacturer Country
- Malta
- 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
- Nov 13, 2009
- Expiry Date
- Nov 13, 2014
- Cancellation Date
- May 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baxter" light-protected intravenous 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 cf3746e1c652b0a61b8b6bffae65bf7c and manufactured by BAXTER (MALTA) LTD.. The authorized representative in Taiwan is BAXTER HEALTHCARE 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