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Ikang Rotavirus (fecal) antigen rapid test reagent - Taiwan Registration 38ccd39ef6c162dcc2869a486dbf5614

Access comprehensive regulatory information for Ikang Rotavirus (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 38ccd39ef6c162dcc2869a486dbf5614 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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38ccd39ef6c162dcc2869a486dbf5614
Registration Details
Taiwan FDA Registration: 38ccd39ef6c162dcc2869a486dbf5614
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Device Details

Ikang Rotavirus (fecal) antigen rapid test reagent
TW: ่‰พๅบท ่ผช็‹€็—…ๆฏ’(็ณžไพฟ)ๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

38ccd39ef6c162dcc2869a486dbf5614

DHA04600089602

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Polio Virus Serological Reagent (C.3405)".

C Immunology and microbiology

C.3405 Poliomyelitis virus serum reagent

Input;; Chinese goods

Dates and Status

Mar 26, 2010

Mar 26, 2015

Apr 25, 2018

Cancellation Information

Logged out

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