Taiwan FDA registration ef3559b0110f9812092b1838e1fc3377
Bury Heart Marker External Quality Assurance Program (Unsterilized)
TW: "伯瑞"心臟標記外部品保計劃(未滅菌)
Registration details
- Analysis ID
- ef3559b0110f9812092b1838e1fc3377
- Customs Code
- DHA04401260606
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 Heart Marker 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 ef3559b0110f9812092b1838e1fc3377 and manufactured by BIO-RAD LABORATORIES INC.. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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