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"Abbott" Dengue Dengue Immunoglobulin M Test Reagent - Taiwan Registration 92ac27e6f1d0d15d77273d385eff14cb

Access comprehensive regulatory information for "Abbott" Dengue Dengue Immunoglobulin M Test Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 92ac27e6f1d0d15d77273d385eff14cb and manufactured by ABBOTT DIAGNOSTICS KOREA INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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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92ac27e6f1d0d15d77273d385eff14cb
Registration Details
Taiwan FDA Registration: 92ac27e6f1d0d15d77273d385eff14cb
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Device Details

"Abbott" Dengue Dengue Immunoglobulin M Test Reagent
TW: "ไบžๅŸน"็™พ่€Œ้ˆ็™ป้ฉ็†ฑๅ…็–ซ็ƒ่›‹็™ฝMๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2

Registration Details

92ac27e6f1d0d15d77273d385eff14cb

DHA05602681208

Company Information

Korea, Republic of

Product Details

Enzyme immunosorbent assay was used to qualitatively detect IgM antibodies to dengue virus in human serum.

C Immunology and microbiology

C.0002 ็™ป้ฉ็†ฑ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 10, 2014

Dec 10, 2029