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“GenBody” Influenza A&B Ag (Non-Sterile) - Taiwan Registration 42c7aa90ca47644773e20923c7015849

Access comprehensive regulatory information for “GenBody” Influenza A&B Ag (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42c7aa90ca47644773e20923c7015849 and manufactured by GENBODY INC.. The authorized representative in Taiwan is EVERMEDICAL COMPANY 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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42c7aa90ca47644773e20923c7015849
Registration Details
Taiwan FDA Registration: 42c7aa90ca47644773e20923c7015849
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Device Details

“GenBody” Influenza A&B Ag (Non-Sterile)
TW: “基因巴帝”流感病毒A&B抗原快速檢驗試劑(未滅菌)
Risk Class 1
MD

Registration Details

42c7aa90ca47644773e20923c7015849

Ministry of Health Medical Device Import No. 019830

DHA09401983000

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Nov 19, 2018

Nov 19, 2023