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"AnyCare" Influenza A/B Rapid Test (Non-Sterile) - Taiwan Registration b92209c12e74f81a19f90d66fbf48ffd

Access comprehensive regulatory information for "AnyCare" Influenza A/B 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 b92209c12e74f81a19f90d66fbf48ffd and manufactured by Asia Genomics Technology Co., Ltd. Factory 1. The authorized representative in Taiwan is Asia Genomics Technology Co., Ltd. Factory 1.

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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b92209c12e74f81a19f90d66fbf48ffd
Registration Details
Taiwan FDA Registration: b92209c12e74f81a19f90d66fbf48ffd
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Device Details

"AnyCare" Influenza A/B Rapid Test (Non-Sterile)
TW: "้—œๅฟƒๆ‚จ" A/Bๅž‹ๆตๆ„Ÿๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b92209c12e74f81a19f90d66fbf48ffd

Ministry of Health Medical Device Manufacturing No. 007118

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 12, 2018

Feb 12, 2023