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"Tauns" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile) - Taiwan Registration 281ec7255be56140c026347926fc91ff

Access comprehensive regulatory information for "Tauns" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (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 281ec7255be56140c026347926fc91ff and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY CO., 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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281ec7255be56140c026347926fc91ff
Registration Details
Taiwan FDA Registration: 281ec7255be56140c026347926fc91ff
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Device Details

"Tauns" Capilia Flu Neo Influenza A&B Virus Antigen Rapid Test (Non-Sterile)
TW: "่—คๅธ" ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’Aๅž‹่ˆ‡Bๅž‹ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

281ec7255be56140c026347926fc91ff

Ministry of Health Medical Device Import No. 016643

DHA09401664302

Company Information

Japan

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

Jun 14, 2016

Jun 14, 2021