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Akon adenovirus (fecal) antigen rapid test reagent - Taiwan Registration 73a0f6cea0d3a63046bc367c1c886f51

Access comprehensive regulatory information for Akon adenovirus (fecal) antigen rapid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 73a0f6cea0d3a63046bc367c1c886f51 and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is Ariel Health Inc.

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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73a0f6cea0d3a63046bc367c1c886f51
Registration Details
Taiwan FDA Registration: 73a0f6cea0d3a63046bc367c1c886f51
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Device Details

Akon adenovirus (fecal) antigen rapid test reagent
TW: ่‰พๅบท ่…บ็—…ๆฏ’(็ณžไพฟ)ๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

73a0f6cea0d3a63046bc367c1c886f51

DHA04600089500

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Chinese goods;; input

Dates and Status

Mar 26, 2010

Mar 26, 2015

Apr 25, 2018

Cancellation Information

Logged out

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