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Qui-visual chorionic gonadotropin assay reagent - Taiwan Registration d081393705c2943abd92683caa025eca

Access comprehensive regulatory information for Qui-visual chorionic gonadotropin assay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d081393705c2943abd92683caa025eca and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIOMERIEUX CHINA LIMITED, TAIWAN BRANCH (HONG KONG).

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d081393705c2943abd92683caa025eca
Registration Details
Taiwan FDA Registration: d081393705c2943abd92683caa025eca
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Device Details

Qui-visual chorionic gonadotropin assay reagent
TW: ๅฅŽๅฏ่ฆ–็ตจๆฏ›่†œไฟƒๆ€ง่…บๆฟ€็ด ๆธฌๅฎš่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

d081393705c2943abd92683caa025eca

DHA00601946401

Company Information

United States

Product Details

Antibody antigen enzyme immune response to test human chorionic gonadotropin in serum or urine.

A Clinical chemistry and clinical toxicology

A.1155 Human chorionic gonadotropin testing system

import

Dates and Status

Oct 22, 2008

Oct 22, 2013

Aug 13, 2015

Cancellation Information

Logged out

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