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QuickVue Influenza A+B Test - Taiwan Registration 2bac9cf885d1366740626354d9ef514f

Access comprehensive regulatory information for QuickVue Influenza A+B Test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2bac9cf885d1366740626354d9ef514f and manufactured by QUIDEL CORPORATION. The authorized representative in Taiwan is BIO-CHECK LABORATORIES LTD..

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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2bac9cf885d1366740626354d9ef514f
Registration Details
Taiwan FDA Registration: 2bac9cf885d1366740626354d9ef514f
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Device Details

QuickVue Influenza A+B Test
TW: โ€œ้€Ÿๅˆฉโ€ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’Aๅž‹ๅ’ŒBๅž‹ๆธฌๅฎš่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

2bac9cf885d1366740626354d9ef514f

Ministry of Health Medical Device Import No. 033508

DHA05603350809

Company Information

United States

Product Details

This product is a rapid qualitative test of influenza virus type A and B antigens used in nasal swabs, nasopharyngeal swabs, nasal aspiration fluid and nasal irrigation fluid samples.

C Immunology and microbiology devices

C3328 Influenza Virus Antigen Rapid Screening System

Imported from abroad

Dates and Status

Jul 17, 2020

Jul 17, 2025