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Redanorovirus rapid test panel - Taiwan Registration 0bd8eca30580574e2c185b958713628d

Access comprehensive regulatory information for Redanorovirus rapid test panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0bd8eca30580574e2c185b958713628d and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is METEK LAB 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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0bd8eca30580574e2c185b958713628d
Registration Details
Taiwan FDA Registration: 0bd8eca30580574e2c185b958713628d
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Device Details

Redanorovirus rapid test panel
TW: ็‘ž้”่ซพ็พ…็—…ๆฏ’ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘็ต„
Risk Class 2
Cancelled

Registration Details

0bd8eca30580574e2c185b958713628d

DHA00602400604

Company Information

Germany

Product Details

A rapid qualitative immunochromatographic analysis test to detect the gene group of Novak virus 1 (GG1) and gene group 2 (GG2) in stool samples.

C Immunology and microbiology

C.3470 ๅ‘ผ่…ธๅญค็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Sep 05, 2012

Sep 05, 2017

Nov 28, 2019

Cancellation Information

Logged out

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