Taiwan FDA registration 4ef8a42edc7d2fdb9a64fc27f29cb0d2
"Baxter" kidney artificial kidney
TW: “百特”利腎人工腎臟
Taiwan·Risk Class 2·NIPRO CORPORATION ODATE FACTORY;; Baxter Healthcare SA·Registered Aug 13, 2013 – Aug 13, 2018CancelledRegistration details
- Analysis ID
- 4ef8a42edc7d2fdb9a64fc27f29cb0d2
- Customs Code
- DHA05602537102
Company information
- Manufacturer Country
- Switzerland;;Japan
- Authorized Representative
- BAXTER HEALTHCARE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5860 高滲透性之血液透析系統
- Import Information
- Chinese goods;; Input;; Contract manufacturing
Dates and status
- Registration Date
- Aug 13, 2013
- Expiry Date
- Aug 13, 2018
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Baxter" kidney artificial kidney in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ef8a42edc7d2fdb9a64fc27f29cb0d2 and manufactured by NIPRO CORPORATION ODATE FACTORY;; Baxter Healthcare SA. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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