Taiwan FDA registration 2f9337060595018dcf313926372997b5
"Shengchuang" Fenix Blood Separation Advanced Set
TW: “笙創”芬尼克斯血液分離進階套組
Taiwan·Risk Class 2·Shengchuang Co., Ltd.; Shengte Technology Co., Ltd·Registered Sep 23, 2023 – Sep 23, 2028ActiveRegistration details
- Analysis ID
- 2f9337060595018dcf313926372997b5
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SAFETRAN BIOMEDICAL INC.
Product details
- Intended Use
- In order to cooperate with the "Shengchuang" Fenix blood apheresis equipment, the relevant consumables required for the blood separation process are provided.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9245 Automated hemocytoseparator
- Import Information
- 委託製造;; 國產;; QMS/QSD
Dates and status
- Registration Date
- Sep 23, 2023
- Expiry Date
- Sep 23, 2028
About this record
Access comprehensive regulatory information for "Shengchuang" Fenix Blood Separation Advanced Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f9337060595018dcf313926372997b5 and manufactured by Shengchuang Co., Ltd.; Shengte Technology Co., Ltd. The authorized representative in Taiwan is SAFETRAN BIOMEDICAL INC..
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