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“Siloam” Rotavirus (Non-Sterile) - Taiwan Registration b8feec8f3d06ecbcfa8c6654fca37985

Access comprehensive regulatory information for “Siloam” Rotavirus (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 b8feec8f3d06ecbcfa8c6654fca37985 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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b8feec8f3d06ecbcfa8c6654fca37985
Registration Details
Taiwan FDA Registration: b8feec8f3d06ecbcfa8c6654fca37985
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Device Details

“Siloam” Rotavirus (Non-Sterile)
TW: “西羅亞” 輪狀病毒快速檢驗試劑 (未滅菌)
Risk Class 1
MD

Registration Details

b8feec8f3d06ecbcfa8c6654fca37985

Ministry of Health Medical Device Import No. 016984

DHA09401698402

Company Information

United States

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

Sep 09, 2016

Sep 09, 2021