"Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza Rapid Test Kit (Unsterilized) - Taiwan Registration c7aabba4fa70aa365837b93dce29330c
Access comprehensive regulatory information for "Ai Kuailu" Respiratory Fusion Cell Virus/A+B Influenza 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 c7aabba4fa70aa365837b93dce29330c and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..
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)" and "Respiratory Fusion Cell Virus Serum Reagent (C.3480)".
C Immunology and microbiology
C.3330 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ;; C.3480 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ
import
Dates and Status
Jul 04, 2018
Jul 04, 2023

