Taiwan FDA registration bd32c36965e655ab8260c61acec87066
"Burry" Blood Coagulation External Quality Assurance Program (Unsterilized)
TW: “伯瑞”血液凝固外部品保計劃(未滅菌)
Taiwan·Risk Class 1·BIO-RAD LABORATORIES INC.·Registered Nov 01, 2012 – Nov 01, 2027ActiveRegistration details
- Analysis ID
- bd32c36965e655ab8260c61acec87066
- Customs Code
- DHA04401233004
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
- Nov 01, 2012
- Expiry Date
- Nov 01, 2027
About this record
Access comprehensive regulatory information for "Burry" Blood Coagulation 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 bd32c36965e655ab8260c61acec87066 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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