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"Artron" Helicobacter Pylori Reagents (Non-sterile) - Taiwan Registration ca7690d7d314ae0a5f469536dd570f46

Access comprehensive regulatory information for "Artron" Helicobacter Pylori Reagents (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca7690d7d314ae0a5f469536dd570f46 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE 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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ca7690d7d314ae0a5f469536dd570f46
Registration Details
Taiwan FDA Registration: ca7690d7d314ae0a5f469536dd570f46
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Device Details

"Artron" Helicobacter Pylori Reagents (Non-sterile)
TW: "้›…ๅ‰ต" ๅนฝ้–€ๆกฟ่Œ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ca7690d7d314ae0a5f469536dd570f46

Ministry of Health Medical Device Import No. 018873

DHA09401887300

Company Information

Canada

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 devices

C0003 Helicobacter serological reagent

Imported from abroad

Dates and Status

Mar 07, 2018

Mar 07, 2023