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Kaiwo Technology Helicobacter pylori test kit (IV) - Taiwan Registration 501f48d64acef50693d890d9be764bca

Access comprehensive regulatory information for Kaiwo Technology Helicobacter pylori test kit (IV) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 501f48d64acef50693d890d9be764bca and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.

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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501f48d64acef50693d890d9be764bca
Registration Details
Taiwan FDA Registration: 501f48d64acef50693d890d9be764bca
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Device Details

Kaiwo Technology Helicobacter pylori test kit (IV)
TW: ้–‹็‰ฉ็ง‘ๆŠ€ๅนฝ้–€่žบๆ—‹ๆกฟ่Œๆชขๆธฌ่ฉฆๅŠ‘็›’(IV)
Risk Class 1
Cancelled

Registration Details

501f48d64acef50693d890d9be764bca

DHA04400617608

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".

C Immunology and microbiology

C.0003 ่žบๆ—‹ๆกฟ่Œๅฑฌ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Sep 26, 2007

Sep 26, 2012

May 05, 2014

Cancellation Information

Logged out

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