Taiwan FDA registration 398d2e2989079ab2fdd673947fe4cc5b

Adenovirus Antigen Rapid Test Reagent (Unsterilized)

TW: 聯華腺病毒抗原快速檢測試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FIRSTEP BIORESEARCH INC.·Registered Jan 18, 2010 – Jan 18, 2030Active
Registration details
Analysis ID
398d2e2989079ab2fdd673947fe4cc5b
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
FIRSTEP BIORESEARCH INC.
Product details
Intended Use
Limited to the first level identification range of the classification and grading management method of medical equipment "adenovirus serum reagent (C.3020)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3020 腺病毒血清試劑
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Jan 18, 2010
Expiry Date
Jan 18, 2030
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About this record

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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