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"Torch" Cardili Mycobacterium tuberculosis rapid identification reagent (unsterilized) - Taiwan Registration cfa4c8d282a0d2b51871d2eeb8a1424c

Access comprehensive regulatory information for "Torch" Cardili Mycobacterium tuberculosis rapid identification 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 cfa4c8d282a0d2b51871d2eeb8a1424c and manufactured by TAUNS LABORATORIES, INC.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TAUNS LABORATORIES, INC., and 1 recent registrations in the same category. 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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cfa4c8d282a0d2b51871d2eeb8a1424c
Registration Details
Taiwan FDA Registration: cfa4c8d282a0d2b51871d2eeb8a1424c
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Device Details

"Torch" Cardili Mycobacterium tuberculosis rapid identification reagent (unsterilized)
TW: "็‚ฌๅˆ" ๅกๅธๅˆฉ ็ตๆ ธๆกฟ่Œ็พคๅฟซ้€Ÿ้‘‘ๅฎš่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

cfa4c8d282a0d2b51871d2eeb8a1424c

DHA04401319302

Company Information

Product Details

Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.

C Immunology and microbiology

C.3370 ็ตๆ ธๆกฟ่Œๅ…็–ซ่žขๅ…‰่ฉฆๅŠ‘

import

Dates and Status

Jul 10, 2013

Jul 10, 2023

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