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Abbott "Marisi" human immunodeficiency virus antibody test reagent - Taiwan Registration 532c7c29bb287f5fcc5d9fbd20fb10e7

Access comprehensive regulatory information for Abbott "Marisi" human immunodeficiency virus antibody 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 532c7c29bb287f5fcc5d9fbd20fb10e7 and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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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532c7c29bb287f5fcc5d9fbd20fb10e7
Registration Details
Taiwan FDA Registration: 532c7c29bb287f5fcc5d9fbd20fb10e7
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Device Details

Abbott "Marisi" human immunodeficiency virus antibody test reagent
TW: ไบžๅŸนโ€ๅฆ™่Šฎ็ตฒโ€ไบบ้กžๅ…็–ซ็ผบไน็—…ๆฏ’ๆŠ—้ซ”ๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 3

Registration Details

532c7c29bb287f5fcc5d9fbd20fb10e7

DHA00601173801

Company Information

Product Details

Enzyme immunoassay for statutory testing of human immunodeficiency virus type 1 and type 2 antibodies in human serum or plasma for screening.

B Hematology, pathology, and genetics

import

Dates and Status

Aug 08, 2005

Aug 08, 2027