Taiwan FDA registration f8e125092d4cc6aca2b06308fad943f1
"Shujiang" HDL cholesterol reagent kit (unsterilized)
TW: "朕江" 高密度脂蛋白膽固醇試劑套組(未滅菌)
Taiwan·Risk Class 1·LANNER BIOTECHNOLOGY CO., LTD.·Registered Sep 08, 2022 – Sep 08, 2027ActiveRegistration details
- Analysis ID
- f8e125092d4cc6aca2b06308fad943f1
Company information
- Manufacturer
- LANNER BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LANNER BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, lipoprotein test system (A.1475) first level recognition range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1475 Lipoprotein Testing System
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Sep 08, 2022
- Expiry Date
- Sep 08, 2027
About this record
Access comprehensive regulatory information for "Shujiang" HDL cholesterol reagent kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f8e125092d4cc6aca2b06308fad943f1 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..
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