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"Artron" Adenovirus Test Kit (Non-sterile) - Taiwan Registration eea0d807dc319a7942385b10bc6c99a2

Access comprehensive regulatory information for "Artron" Adenovirus Test Kit (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 eea0d807dc319a7942385b10bc6c99a2 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is YOULUM BIOTECHNOLOGY 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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eea0d807dc319a7942385b10bc6c99a2
Registration Details
Taiwan FDA Registration: eea0d807dc319a7942385b10bc6c99a2
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Device Details

"Artron" Adenovirus Test Kit (Non-sterile)
TW: "่‰พๅ‰ต"่…บ็—…ๆฏ’ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

eea0d807dc319a7942385b10bc6c99a2

Ministry of Health Medical Device Import No. 014911

DHA09401491101

Company Information

Canada

Product Details

C Immunology and microbiology devices

C3020 adenovirus serum reagent

Imported from abroad

Dates and Status

Feb 10, 2015

Feb 10, 2020

Sep 25, 2019

Cancellation Information

Logged out

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