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"Artron" Rotavirus Test Kit (Non-Sterile) - Taiwan Registration 1d9b397d64c595ce53943bac465b63a8

Access comprehensive regulatory information for "Artron" Rotavirus 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 1d9b397d64c595ce53943bac465b63a8 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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1d9b397d64c595ce53943bac465b63a8
Registration Details
Taiwan FDA Registration: 1d9b397d64c595ce53943bac465b63a8
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Device Details

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

Registration Details

1d9b397d64c595ce53943bac465b63a8

Ministry of Health Medical Device Import No. 014912

DHA09401491203

Company Information

Canada

Product Details

C Immunology and microbiology devices

C3405 Polio virus serum reagent

Imported from abroad

Dates and Status

Feb 10, 2015

Feb 10, 2020

Oct 02, 2019

Cancellation Information

Logged out

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