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"Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 test reagent - Taiwan Registration 0c60f1c32c1bea4537d9118bd3aded83

Access comprehensive regulatory information for "Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0c60f1c32c1bea4537d9118bd3aded83 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..

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0c60f1c32c1bea4537d9118bd3aded83
Registration Details
Taiwan FDA Registration: 0c60f1c32c1bea4537d9118bd3aded83
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Device Details

"Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 test reagent
TW: โ€œๆ–ฐ็ง‘ๅŒ–โ€ ไบบ้กžๅ…็–ซ็ผบไน็—…ๆฏ’ๆŠ—้ซ”่ฅฟๆ–นๅขจ้ปžๆณ•2.2ๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 3
Cancelled

Registration Details

0c60f1c32c1bea4537d9118bd3aded83

DHA00602384706

Company Information

Product Details

Western ink dot testing for HIV-1 and HIV-2 antibodies in human serum or plasma can be used as a confirmation reagent for HIV-1, and HIV-2 positive patients should be confirmed with other reagents.

B Hematology, pathology, and genetics

B.4020 Analysis of specific tests

import

Dates and Status

Aug 16, 2012

Apr 07, 2014

Nov 15, 2016

Cancellation Information

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