"Siloa" Respiratory Fusion Cell Virus and Adenovirus Rapid Test Reagent (Unsterilized) - Taiwan Registration 7d1ec4026d45011ff02a8ef561f1023c
Access comprehensive regulatory information for "Siloa" Respiratory Fusion Cell Virus and Adenovirus 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 7d1ec4026d45011ff02a8ef561f1023c and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is Siloam Biotech 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
It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" and "Respiratory Fusion Cell Virus Serum Reagent (C.3480)" in the Classification and Grading Management Measures for Medical Devices.
C Immunology and microbiology
C.3480 ๅผๅธ้่ๅ็ดฐ่็ ๆฏ่กๆธ ่ฉฆๅ;; C.3020 ่ บ็ ๆฏ่กๆธ ่ฉฆๅ
Input;; Chinese goods
Dates and Status
Apr 28, 2021
Apr 28, 2026

