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Orien "Peroria" dry pylori reagent - Taiwan Registration 3956c1efb13757ab52ddf210356b19ba

Access comprehensive regulatory information for Orien "Peroria" dry pylori reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3956c1efb13757ab52ddf210356b19ba and manufactured by ORION DIAGNOSTICA LTD. The authorized representative in Taiwan is HOPE WANG ENTERPRISES CO., LTD..

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3956c1efb13757ab52ddf210356b19ba
Registration Details
Taiwan FDA Registration: 3956c1efb13757ab52ddf210356b19ba
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Device Details

Orien "Peroria" dry pylori reagent
TW: ๆญ้Šณๆฉใ€ๆดพ็พ…็‘žใ€žไนพๅผๅนฝ้–€ๆกฟ่Œ่ฉฆๅŠ‘
Risk Class 1
Cancelled

Registration Details

3956c1efb13757ab52ddf210356b19ba

DHA04400124808

Company Information

Finland

Product Details

Latex rapid agglutination was used to qualitatively detect Helicobacter pylobacter antibodies in human serum.

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 26, 2005

Oct 26, 2015

May 28, 2018

Cancellation Information

Logged out

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