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"CJ" A/B Influenza Rapid Test (Non-sterile) - Taiwan Registration 45b81b04864d9495de6e55164de4f094

Access comprehensive regulatory information for "CJ" A/B Influenza 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 45b81b04864d9495de6e55164de4f094 and manufactured by Qizhe Biotechnology Co., Ltd. The authorized representative in Taiwan is Qizhe 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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45b81b04864d9495de6e55164de4f094
Registration Details
Taiwan FDA Registration: 45b81b04864d9495de6e55164de4f094
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Device Details

"CJ" A/B Influenza Rapid Test (Non-sterile)
TW: "ๅ•Ÿๅ“ฒ"A/Bๅž‹ๆต่กŒๆ€งๆ„Ÿๅ†’็—…ๆฏ’ๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

45b81b04864d9495de6e55164de4f094

Ministry of Health Medical Device Manufacturing No. 007656

Company Information

Taiwan, Province of China

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

Produced in Taiwan, China

Dates and Status

Feb 20, 2019

Feb 20, 2024