Taiwan FDA registration ddc6e9093dca2e2bddd15b9310258598
"Baxter" infusion sleeve
TW: "百特" 輸液套
Taiwan·Risk Class 2·BAXTER PRODUCTOS MEDICOS LTDA;; BAXTER HEALTHCARE CORPORATION·Registered Sep 05, 2002 – Sep 05, 2017CancelledRegistration details
- Analysis ID
- ddc6e9093dca2e2bddd15b9310258598
- Customs Code
- DHA00601006201
Company information
- Manufacturer Country
- Costa Rica;;United States
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- Vacuum.
- 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
- Sep 05, 2002
- Expiry Date
- Sep 05, 2017
- Cancellation Date
- Nov 21, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Baxter" infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ddc6e9093dca2e2bddd15b9310258598 and manufactured by BAXTER PRODUCTOS MEDICOS LTDA;; BAXTER HEALTHCARE CORPORATION. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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