Taiwan FDA registration 44d37fe17a4a8371f99f654b3d55233c
"Burry" Blood Typing External Quality Assurance Program (Unsterilized)
TW: "伯瑞" 血液分型外部品保計畫 (未滅菌)
Taiwan·Risk Class 1·BIO-RAD LABORATORIES INC.·Registered May 20, 2016 – May 20, 2026ExpiredRegistration details
- Analysis ID
- 44d37fe17a4a8371f99f654b3d55233c
- Customs Code
- DHA09401656301
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
- May 20, 2016
- Expiry Date
- May 20, 2026
About this record
Access comprehensive regulatory information for "Burry" Blood Typing External Quality Assurance Program (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 44d37fe17a4a8371f99f654b3d55233c 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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