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“QIAGEN” artus EBV QS-RGQ Kit (Non-sterile) - Taiwan Registration fcdd1f0b06b1f832a8375e1ef0f993e1

Access comprehensive regulatory information for “QIAGEN” artus EBV QS-RGQ Kit (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 fcdd1f0b06b1f832a8375e1ef0f993e1 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

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fcdd1f0b06b1f832a8375e1ef0f993e1
Registration Details
Taiwan FDA Registration: fcdd1f0b06b1f832a8375e1ef0f993e1
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Device Details

“QIAGEN” artus EBV QS-RGQ Kit (Non-sterile)
TW: “凱杰” 阿特斯 EB 病毒核酸檢驗試劑組 (未滅菌)
Risk Class 1
MD

Registration Details

fcdd1f0b06b1f832a8375e1ef0f993e1

Ministry of Health Medical Device Import No. 021622

DHA09402162201

Company Information

Germany

Product Details

Limited to the first level identification range of "Epstein-Barr virus serum reagent (C.3235)" of the Measures for the Administration of Medical Devices.

C Immunology and microbiology devices

C3235 Epstein-Barr virus serum reagent

Imported from abroad

Dates and Status

Jun 05, 2020

Jun 05, 2025