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"Dias" Helicobacter pylori IgG antibody detection kit (unsterilized) - Taiwan Registration acce8a4f41fccd0c915ffd0aca233399

Access comprehensive regulatory information for "Dias" Helicobacter pylori IgG 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 acce8a4f41fccd0c915ffd0aca233399 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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acce8a4f41fccd0c915ffd0aca233399
Registration Details
Taiwan FDA Registration: acce8a4f41fccd0c915ffd0aca233399
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Device Details

"Dias" Helicobacter pylori IgG antibody detection kit (unsterilized)
TW: "่ฟช้›…ไป•" ๅฏ้Œ„ๆ€ ๅนฝ้–€่žบๆ—‹ๆกฟ่ŒIgGๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

acce8a4f41fccd0c915ffd0aca233399

DHA04401254502

Company Information

Product Details

Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Jan 04, 2013

Jan 04, 2028