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Rapid Test Reagent for Influenza Virus A and B (Unsterilized) - Taiwan Registration 3f49279c01150054b056e1c1d0e5409e

Access comprehensive regulatory information for Rapid Test Reagent for Influenza Virus A and B (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f49279c01150054b056e1c1d0e5409e and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.

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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3f49279c01150054b056e1c1d0e5409e
Registration Details
Taiwan FDA Registration: 3f49279c01150054b056e1c1d0e5409e
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Device Details

Rapid Test Reagent for Influenza Virus A and B (Unsterilized)
TW: ้†ซ่ฉฆ็พŽๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’Aๅž‹ๅŠBๅž‹ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

3f49279c01150054b056e1c1d0e5409e

Company Information

Taiwan, Province of China

Product Details

It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.

C Immunology and microbiology

C.3330 ๆตๆ„Ÿ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Domestic

Dates and Status

Jan 27, 2014

Jan 27, 2024