Taiwan FDA registration 634d52224fd056c9273264277824afc2
"Xingchang" plasma filtration waste bag (unsterilized)
TW: “杏昌”血漿過濾廢液袋 (未滅菌)
Taiwan·Risk Class 1·VITAL HEALTHCARE SDN BHD·Registered Apr 08, 2019 – Apr 08, 2024ExpiredRegistration details
- Analysis ID
- 634d52224fd056c9273264277824afc2
- Customs Code
- DHA09402027702
Company information
- Manufacturer
- VITAL HEALTHCARE SDN BHD
- Manufacturer Country
- Malaysia
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- It is limited to the scope of the first level of identification of the "Hemodialysis System and Its Accessories (H.5820)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5820 血液透析系統及其附件
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Apr 08, 2019
- Expiry Date
- Apr 08, 2024
About this record
Access comprehensive regulatory information for "Xingchang" plasma filtration waste bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 634d52224fd056c9273264277824afc2 and manufactured by VITAL HEALTHCARE SDN BHD. The authorized representative in Taiwan is HI-CLEARANCE INC..
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