Taiwan FDA registration 8253cd12033512eaf2b26a1b3be74c41
"Baxter" automatic peritoneal dialysis machine connection platform
TW: “百特”全自動腹膜透析機連線平台
Taiwan·Risk Class 2·Baxter Healthcare Corporation Medical Products;; Baxter Healthcare SA·Registered Oct 16, 2017 – Oct 16, 2027ActiveRegistration details
- Analysis ID
- 8253cd12033512eaf2b26a1b3be74c41
- Customs Code
- DHA05603034709
Company information
- Manufacturer Country
- United States;;Switzerland
- 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.5630 腹膜透析系統及其附件
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Oct 16, 2017
- Expiry Date
- Oct 16, 2027
About this record
Access comprehensive regulatory information for "Baxter" automatic peritoneal dialysis machine connection platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8253cd12033512eaf2b26a1b3be74c41 and manufactured by Baxter Healthcare Corporation Medical Products;; Baxter Healthcare SA. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
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