Baynex Respiratory Fusion Viral Antigen Rapid Diagnostic Test Card (Unsterilized) - Taiwan Registration 522535a27e2221a7c9955cd0233dde8e
Access comprehensive regulatory information for Baynex Respiratory Fusion Viral Antigen Rapid Diagnostic Test Card (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 522535a27e2221a7c9955cd0233dde8e and manufactured by Abbott Diagnostics Scarborough, Inc.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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Device Details
Product Details
Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".
C Immunology and microbiology
C.3480 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ
import
Dates and Status
Jul 18, 2012
Jul 18, 2027