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"Deas" Helicobacter pylori IgA Antibody Detection Kit (Unsterilized) - Taiwan Registration 10df013a4c1d9e6c6455e94300e79a37

Access comprehensive regulatory information for "Deas" Helicobacter pylori IgA 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 10df013a4c1d9e6c6455e94300e79a37 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A. The authorized representative in Taiwan is Grand Marquis IVD 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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10df013a4c1d9e6c6455e94300e79a37
Registration Details
Taiwan FDA Registration: 10df013a4c1d9e6c6455e94300e79a37
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Device Details

"Deas" Helicobacter pylori IgA Antibody Detection Kit (Unsterilized)
TW: "่ฟช้›…ไป•" ๅฏ้Œ„ๆ€ ๅนฝ้–€่žบๆ—‹ๆกฟ่Œ IgA ๆŠ—้ซ”ๆชขๆธฌ่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

10df013a4c1d9e6c6455e94300e79a37

DHA04401255005

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‘

Input;; QMS/QSD

Dates and Status

Jan 07, 2013

Jan 07, 2028