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DENKA Quick Navi-Flu2 (Non-Sterile) - Taiwan Registration 22342e644dbbddbc3851b78801b3420a

Access comprehensive regulatory information for DENKA Quick Navi-Flu2 (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 22342e644dbbddbc3851b78801b3420a and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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22342e644dbbddbc3851b78801b3420a
Registration Details
Taiwan FDA Registration: 22342e644dbbddbc3851b78801b3420a
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Device Details

DENKA Quick Navi-Flu2 (Non-Sterile)
TW: ็”Ÿ็ ”ๅฟซ็ดๅจๆต่กŒๆ€งๆ„Ÿๅ†’ๅฟซ้€Ÿๆชข้ฉ—ๅฅ—็ต„็ฌฌไบŒไปฃ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

22342e644dbbddbc3851b78801b3420a

Ministry of Health Medical Device Import No. 018531

DHA09401853101

Company Information

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 21, 2017

Nov 21, 2022