Fiquor A+B Influenza Rapid Test Reagent (Unsterilized) - Taiwan Registration 2eb0cf736522673a99d2698ce7df13c1
Access comprehensive regulatory information for Fiquor A+B Influenza Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2eb0cf736522673a99d2698ce7df13c1 and manufactured by Baoling Fujin Biotechnology Co., Ltd. Xizhi Factory. The authorized representative in Taiwan is PANION & BF BIOTECH INC..
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 Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
C Immunology and microbiology
C.3330 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ
Domestic
Dates and Status
Oct 29, 2015
Oct 29, 2020
Jul 15, 2022
Cancellation Information
Logged out
ๆชๅฑๅปถ่้พๆ่