Taiwan FDA registration 9716bdfdfb46ee959b9320450800d312
"Bury" Ethanol/Ammonia External Quality Assurance Program (Unsterilized)
TW: "伯瑞"乙醇/氨外部品保計劃(未滅菌)
Taiwan·Risk Class 1·BIO-RAD LABORATORIES INC.·Registered Jan 17, 2013 – Jan 17, 2028ActiveRegistration details
- Analysis ID
- 9716bdfdfb46ee959b9320450800d312
- Customs Code
- DHA04401260708
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
- import
Dates and status
- Registration Date
- Jan 17, 2013
- Expiry Date
- Jan 17, 2028
About this record
Access comprehensive regulatory information for "Bury" Ethanol/Ammonia 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 9716bdfdfb46ee959b9320450800d312 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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