Bio-Research Rapid Test Kit for Influenza and Respiratory Fusion Cell Virus (Unsterilized) - Taiwan Registration 0c1795622d8796426ffa2e4f4ff97dde
Access comprehensive regulatory information for Bio-Research Rapid Test Kit for Influenza and Respiratory Fusion Cell 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 0c1795622d8796426ffa2e4f4ff97dde and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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
It is limited to the first-level identification scope of the "Respiratory Fusion Cell Virus Serum Reagent (C.3480)" and "Influenza Virus Serum Reagent (C.3330)" of the Classification and Grading Management Measures for Medical Devices.
C Immunology and microbiology
C.3480 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ;; C.3330 ๆตๆ็ ๆฏ่กๆธ ่ฉฆๅ
import
Dates and Status
May 15, 2014
May 15, 2024

