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"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.

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7d1ec4026d45011ff02a8ef561f1023c
Registration Details
Taiwan FDA Registration: 7d1ec4026d45011ff02a8ef561f1023c
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Device Details

"Siloa" Respiratory Fusion Cell Virus and Adenovirus Rapid Test Reagent (Unsterilized)
TW: "่ฅฟ็พ…ไบž" ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’ๅŠ่…บ็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7d1ec4026d45011ff02a8ef561f1023c

DHA09600451401

Company Information

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 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; Chinese goods

Dates and Status

Apr 28, 2021

Apr 28, 2026