Taiwan FDA registration 78c42e720d227ed65a684c3149be0d23

Adenovirus antigen rapid test reagent (unsterilized)

TW: “凌越”腺病毒抗原快速檢驗試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Lingyue Biomedical Co., Ltd. Taipei Factory·Registered Aug 26, 2013 – Aug 26, 2018Cancelled
Registration details
Analysis ID
78c42e720d227ed65a684c3149be0d23
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological 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
Domestic
Dates and status
Registration Date
Aug 26, 2013
Expiry Date
Aug 26, 2018
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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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 78c42e720d227ed65a684c3149be0d23 and manufactured by Lingyue Biomedical Co., Ltd. Taipei Factory. The authorized representative in Taiwan is Lingyue Biomedical Co., Ltd. Taipei Factory.

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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