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"RapiGEN" Flu (Non-Sterile) - Taiwan Registration 03ea532ddb9dffd0dee79f9879a8c091

Access comprehensive regulatory information for "RapiGEN" Flu (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 03ea532ddb9dffd0dee79f9879a8c091 and manufactured by RAPIGEN INC.. The authorized representative in Taiwan is Jingpeng Limited.

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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03ea532ddb9dffd0dee79f9879a8c091
Registration Details
Taiwan FDA Registration: 03ea532ddb9dffd0dee79f9879a8c091
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Device Details

"RapiGEN" Flu (Non-Sterile)
TW: ใ€็‘ž่ปใ€žๆตๆ„Ÿ็—…ๆฏ’A&BๆŠ—ๅŽŸๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

03ea532ddb9dffd0dee79f9879a8c091

Ministry of Health Medical Device Import No. 020174

DHA09402017405

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

Mar 12, 2019

Mar 12, 2024