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Mycobacterium tuberculosis asia rapid test kit (unsterilized) - Taiwan Registration 7b17a0199ef5e4dfb696637dbb489ad6

Access comprehensive regulatory information for Mycobacterium tuberculosis asia rapid 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 7b17a0199ef5e4dfb696637dbb489ad6 and manufactured by Asia Genomics Technology Co., Ltd. Factory 1. The authorized representative in Taiwan is Asia Genomics Technology Co., Ltd. Factory 1.

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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7b17a0199ef5e4dfb696637dbb489ad6
Registration Details
Taiwan FDA Registration: 7b17a0199ef5e4dfb696637dbb489ad6
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Device Details

Mycobacterium tuberculosis asia rapid test kit (unsterilized)
TW: ไบžๆดฒๅŸบๅ› ็ตๆ ธๅˆ†ๆžๆกฟ่Œๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7b17a0199ef5e4dfb696637dbb489ad6

DHY04300247507

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment, Mycobacterium tuberculosis immunofluorescent reagent (C.3370) first level identification range.

C Immunology and microbiology

C.3370 ็ตๆ ธๆกฟ่Œๅ…็–ซ่žขๅ…‰่ฉฆๅŠ‘

Domestic

Dates and Status

Jun 03, 2009

Jun 03, 2024