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Cyanidium typhi antigen test reagent (unsterilized) - Taiwan Registration aeef81a3d78ac96c70284ecff8b1e300

Access comprehensive regulatory information for Cyanidium typhi antigen 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 aeef81a3d78ac96c70284ecff8b1e300 and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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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aeef81a3d78ac96c70284ecff8b1e300
Registration Details
Taiwan FDA Registration: aeef81a3d78ac96c70284ecff8b1e300
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Device Details

Cyanidium typhi antigen test reagent (unsterilized)
TW: โ€œ้€Ÿๅธโ€ๅ‚ทๅฏ’ๆฒ™้–€ๆฐ่ŒๆŠ—ๅŽŸๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

aeef81a3d78ac96c70284ecff8b1e300

DHA04400908303

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Salmonella Serological Reagent (C.3550)".

C Immunology and microbiology

C.3550 ๆฒ™้–€ๆฐ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Aug 12, 2010

Aug 12, 2020

Jul 15, 2022

Cancellation Information

Logged out

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