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"All Souls" respiratory fusion virus antigen fluorescence test kit (unsterilized) - Taiwan Registration 8783582acf6261823b5232c4e00750e6

Access comprehensive regulatory information for "All Souls" respiratory fusion virus antigen fluorescence test kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8783582acf6261823b5232c4e00750e6 and manufactured by OXOID LTD.. The authorized representative in Taiwan is WONDERFUL LIFE SCIENCE 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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8783582acf6261823b5232c4e00750e6
Registration Details
Taiwan FDA Registration: 8783582acf6261823b5232c4e00750e6
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Device Details

"All Souls" respiratory fusion virus antigen fluorescence test kit (unsterilized)
TW: "่ฌ้ˆ"ๅ‘ผๅธ้“่žๅˆ็—…ๆฏ’ๆŠ—ๅŽŸ่žขๅ…‰ๆชข้ฉ—่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

8783582acf6261823b5232c4e00750e6

DHA04400942100

Company Information

United Kingdom

Product Details

Limited to the classification and grading management of medical devices, the first level identification range of "respiratory fusion cell virus serum reagent (C.3480)".

C Immunology and microbiology

C.3480 ๅ‘ผๅธ้“่žๅˆ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Oct 27, 2010

Oct 27, 2025