Taiwan FDA registration f6c92f91abaa4af1cfbf122e1f9c3cae
"Bioken" Dense LDL Cholesterol Test Reagent (Unsterilized)
TW: 〝生研〞緻密低密度脂蛋白膽固醇檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·DENKA CO., LTD·Registered Dec 07, 2011 – Dec 07, 2026ActiveRegistration details
- Analysis ID
- f6c92f91abaa4af1cfbf122e1f9c3cae
- Customs Code
- DHA04401115303
Company information
- Manufacturer
- DENKA CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
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
- import
Dates and status
- Registration Date
- Dec 07, 2011
- Expiry Date
- Dec 07, 2026
About this record
Access comprehensive regulatory information for "Bioken" Dense LDL Cholesterol Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f6c92f91abaa4af1cfbf122e1f9c3cae and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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