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"Ichuang" rotavirus/adenovirus 2-in-1 rapid test (unsterilized) - Taiwan Registration b3a08de3a67727a188bddb53dbeaaf55

Access comprehensive regulatory information for "Ichuang" rotavirus/adenovirus 2-in-1 rapid test (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b3a08de3a67727a188bddb53dbeaaf55 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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b3a08de3a67727a188bddb53dbeaaf55
Registration Details
Taiwan FDA Registration: b3a08de3a67727a188bddb53dbeaaf55
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Device Details

"Ichuang" rotavirus/adenovirus 2-in-1 rapid test (unsterilized)
TW: "่‰พๅ‰ต"่ผช็‹€็—…ๆฏ’/่…บ็—…ๆฏ’ไบŒๅˆไธ€ๅฟซ้€Ÿๆชขๆธฌ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b3a08de3a67727a188bddb53dbeaaf55

DHA09401491002

Company Information

Canada

Product Details

Limited to the first level of identification range of "polio virus serum reagent (C.3405)" and "adenovirus serum reagent (C.3020)" under the management measures for medical devices.

C Immunology and microbiology

C.3020 ่…บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘;; C.3405 ๅฐๅ…’้บป็—บ็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

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Dates and Status

Feb 10, 2015

Feb 10, 2020

Sep 25, 2019

Cancellation Information

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