Taiwan FDA registration ba1c161f0f2adf60fb042dcdfd36bec1
"Shengchuang" Fenix blood component separation equipment
TW: “笙創” 芬尼克斯血液成分分離設備
Taiwan·Risk Class 2·Shengchuang Co., Ltd.; Shengte Technology Co., Ltd·Registered Apr 30, 2014 – Apr 30, 2029ActiveRegistration details
- Analysis ID
- ba1c161f0f2adf60fb042dcdfd36bec1
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SAFETRAN BIOMEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9245 Automated hemocytoseparator
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 30, 2014
- Expiry Date
- Apr 30, 2029
About this record
Access comprehensive regulatory information for "Shengchuang" Fenix blood component separation equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba1c161f0f2adf60fb042dcdfd36bec1 and manufactured by Shengchuang Co., Ltd.; Shengte Technology Co., Ltd. The authorized representative in Taiwan is SAFETRAN BIOMEDICAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices