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Adenovirus Antigen Rapid Test Reagent (Unsterilized) - Taiwan Registration 398d2e2989079ab2fdd673947fe4cc5b

Access comprehensive regulatory information for Adenovirus Antigen Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 398d2e2989079ab2fdd673947fe4cc5b and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Asia Genomics Technology Co., Ltd. Factory 1, ABBOTT DIAGNOSTICS MEDICAL CO., LTD.-CHIBA PLANT, and 5 recent registrations in the same category. 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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398d2e2989079ab2fdd673947fe4cc5b
Registration Details
Taiwan FDA Registration: 398d2e2989079ab2fdd673947fe4cc5b
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Device Details

Adenovirus Antigen Rapid Test Reagent (Unsterilized)
TW: ่ฏ่ฏ่…บ็—…ๆฏ’ๆŠ—ๅŽŸๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

398d2e2989079ab2fdd673947fe4cc5b

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the classification and grading management method of medical equipment "adenovirus serum reagent (C.3020)".

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Jan 18, 2010

Jan 18, 2030