PIIP Rapid Detection Reagent for Influenza A/B Virus (Unsterilized) - Taiwan Registration 966989b811aef6a8a13fc7929653eb7e
Access comprehensive regulatory information for PIIP Rapid Detection Reagent for Influenza A/B Virus (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 966989b811aef6a8a13fc7929653eb7e and manufactured by HANGZHOU BIOTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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
Chinese goods;; input
Dates and Status
Jul 26, 2017
Jul 26, 2022
Apr 12, 2024
Cancellation Information
Logged out
่จฑๅฏ่ญๅทฒ้พๆๆๆ