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“SD BIOSENSOR” STANDARD Q Rotavirus Ag Test (Non-Sterile) - Taiwan Registration c8f4504c7f8123b5652cebe84c252c48

Access comprehensive regulatory information for “SD BIOSENSOR” STANDARD Q Rotavirus Ag Test (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 c8f4504c7f8123b5652cebe84c252c48 and manufactured by SD BIOSENSOR, Inc.. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE 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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c8f4504c7f8123b5652cebe84c252c48
Registration Details
Taiwan FDA Registration: c8f4504c7f8123b5652cebe84c252c48
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Device Details

“SD BIOSENSOR” STANDARD Q Rotavirus Ag Test (Non-Sterile)
TW: “速得百森” 輪狀病毒快速檢驗試劑 (未滅菌)
Risk Class 1
MD

Registration Details

c8f4504c7f8123b5652cebe84c252c48

Ministry of Health Medical Device Import No. 022561

DHA09402256109

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Polio Virus Serological Reagent (C.3405)".

C Immunology and microbiology devices

C3405 Polio virus serum reagent

Imported from abroad

Dates and Status

Apr 29, 2021

Apr 29, 2026