"Yi Xinda" A+B influenza virus rapid test kit (unsterilized) - Taiwan Registration ed9ebd9f8edea55dc2e6c12fb31d1760
Access comprehensive regulatory information for "Yi Xinda" A+B influenza virus 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 ed9ebd9f8edea55dc2e6c12fb31d1760 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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Device Details
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
C Immunology and microbiology
C.3330 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ
import
Dates and Status
Aug 24, 2009
Aug 24, 2019
Jun 07, 2022
Cancellation Information
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