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"Siloam" Rotavirus/Adenovirus Combi-test (Non-Sterile) - Taiwan Registration 82d47c8acf2ed2cf468d633fea882267

Access comprehensive regulatory information for "Siloam" Rotavirus/Adenovirus Combi-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 82d47c8acf2ed2cf468d633fea882267 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is Siloam Biotech 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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82d47c8acf2ed2cf468d633fea882267
Registration Details
Taiwan FDA Registration: 82d47c8acf2ed2cf468d633fea882267
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Device Details

"Siloam" Rotavirus/Adenovirus Combi-test (Non-Sterile)
TW: "่ฅฟ็พ…ไบž" ่ผช็‹€็—…ๆฏ’/่…บ็—…ๆฏ’ไบŒๅˆไธ€ๆชข้ฉ—่ฉฆๅŠ‘็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

82d47c8acf2ed2cf468d633fea882267

Ministry of Health Medical Device Import No. 016986

DHA09401698603

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".

C Immunology and microbiology devices

C3020 adenovirus serum reagent

Imported from abroad

Dates and Status

Sep 09, 2016

Sep 09, 2021