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"Dias" Velvis Epstein-Barr virus early antigen IgM antibody detection kit (unsterilized) - Taiwan Registration 9058c2a09358c4cbff8e7f09ee8c2df5

Access comprehensive regulatory information for "Dias" Velvis Epstein-Barr virus early antigen IgM antibody detection 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 9058c2a09358c4cbff8e7f09ee8c2df5 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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9058c2a09358c4cbff8e7f09ee8c2df5
Registration Details
Taiwan FDA Registration: 9058c2a09358c4cbff8e7f09ee8c2df5
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Device Details

"Dias" Velvis Epstein-Barr virus early antigen IgM antibody detection kit (unsterilized)
TW: "่ฟช้›…ไป•" ๅฏ้Œ„ๆ€ EB็—…ๆฏ’ๆ—ฉๆœŸๆŠ—ๅŽŸIgMๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9058c2a09358c4cbff8e7f09ee8c2df5

DHA04401276003

Company Information

Product Details

Limited to the first level identification range of the classification and grading management method for medical devices "Ebr virus serum reagent (C.3235)".

C Immunology and microbiology

C.3235 EB็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

Input;; QMS/QSD

Dates and Status

Mar 01, 2013

Mar 01, 2028