"Bioken" Krivour Adenovirus (Respiratory) Rapid Test Kit (Unsterilized) - Taiwan Registration 850f1630c981b25eb73be3e8c751a1c2
Access comprehensive regulatory information for "Bioken" Krivour Adenovirus (Respiratory) Rapid Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 850f1630c981b25eb73be3e8c751a1c2 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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.
Device Details
Product Details
Limited to the first level identification range of the classification and grading management method of medical equipment "adenovirus serum reagent (C.3020)".
C Immunology and microbiology
C.3020 腺病毒血清試劑
import
Dates and Status
Jun 28, 2012
Jun 28, 2027

