Pure Global

Ikon single-step rotavirus adenovirus 2-in-1 (fecal) antigen rapid test reagent - Taiwan Registration 916850c65a31e8b51e6400c5484f1819

Access comprehensive regulatory information for Ikon single-step rotavirus adenovirus 2-in-1 (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 916850c65a31e8b51e6400c5484f1819 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
916850c65a31e8b51e6400c5484f1819
Registration Details
Taiwan FDA Registration: 916850c65a31e8b51e6400c5484f1819
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Ikon single-step rotavirus adenovirus 2-in-1 (fecal) antigen rapid test reagent
TW: ่‰พๅบท ๅ–ฎไธ€ๆญฅ้ฉŸ่ผช็‹€็—…ๆฏ’่…บ็—…ๆฏ’ไบŒๅˆไธ€(็ณžไพฟ)ๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

916850c65a31e8b51e6400c5484f1819

DHA04600089401

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

่‡ช่กŒ้ตๅ…ฅ