Kaiwo Technology Influenza A and B Kits - Taiwan Registration 139f1f31453f9cc1a7e26b612be2294b
Access comprehensive regulatory information for Kaiwo Technology Influenza A and B Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 139f1f31453f9cc1a7e26b612be2294b and manufactured by HANGZHOU GENESIS BIODETECTION AND BIOCONTROL CO., LTD;; EQUAL ACCESS TO SCIENTIFIC EXCELLENCE. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.
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
Registration Details
139f1f31453f9cc1a7e26b612be2294b
DHA04600078802
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
Contract manufacturing;; Input;; Chinese goods
Dates and Status
Sep 08, 2009
Sep 08, 2014
Jun 25, 2018
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ

