Taiwan FDA registration 5ccd502e186010642fff6f7ad8f26d46
"Burry" Urinalysis External Quality Assurance Program (Unsterilized)
TW: "伯瑞" 尿液分析外部品保計畫 (未滅菌)
Taiwan·Risk Class 1·BIO-RAD LABORATORIES INC.·Registered Jun 23, 2016 – Jun 23, 2026ExpiredRegistration details
- Analysis ID
- 5ccd502e186010642fff6f7ad8f26d46
- Customs Code
- DHA09401668604
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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jun 23, 2016
- Expiry Date
- Jun 23, 2026
About this record
Access comprehensive regulatory information for "Burry" Urinalysis 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 5ccd502e186010642fff6f7ad8f26d46 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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