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"Siloam" Influenza A&B Test (Non-sterile) - Taiwan Registration f17546d024bae39030cb6e5f152cc42a

Access comprehensive regulatory information for "Siloam" Influenza A&B 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 f17546d024bae39030cb6e5f152cc42a 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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f17546d024bae39030cb6e5f152cc42a
Registration Details
Taiwan FDA Registration: f17546d024bae39030cb6e5f152cc42a
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Device Details

"Siloam" Influenza A&B Test (Non-sterile)
TW: "่ฅฟ็พ…ไบž" ๆตๆ„Ÿ็—…ๆฏ’A&Bๅฟซ้€Ÿๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f17546d024bae39030cb6e5f152cc42a

Ministry of Health Medical Device Import No. 016985

DHA09401698501

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".

C Immunology and microbiology devices

C3330 Influenza virus serum reagent

Imported from abroad

Dates and Status

Sep 09, 2016

Sep 09, 2021