Taiwan FDA registration 8769327027955fccfd93ccaf5d22b218
Berry External Quality Assurance Program for HIV/Hepatitis (Unsterilized)
TW: "伯瑞" 愛滋病毒/肝炎外部品保計畫 (未滅菌)
Taiwan·Risk Class 1·BIO-RAD LABORATORIES INC.·Registered Jun 23, 2016 – Jun 23, 2026ExpiredRegistration details
- Analysis ID
- 8769327027955fccfd93ccaf5d22b218
- Customs Code
- DHA09401668706
Company information
- Manufacturer
- BIO-RAD LABORATORIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 23, 2016
- Expiry Date
- Jun 23, 2026
About this record
Access comprehensive regulatory information for Berry External Quality Assurance Program for HIV/Hepatitis (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8769327027955fccfd93ccaf5d22b218 and manufactured by BIO-RAD LABORATORIES INC.. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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