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“QIAGEN” artus BK Virus QS-RGQ kit (Non-sterile) - Taiwan Registration 3bb7208441c760bd1ff4828c4c73a33d

Access comprehensive regulatory information for “QIAGEN” artus BK Virus 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 3bb7208441c760bd1ff4828c4c73a33d and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

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3bb7208441c760bd1ff4828c4c73a33d
Registration Details
Taiwan FDA Registration: 3bb7208441c760bd1ff4828c4c73a33d
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Device Details

“QIAGEN” artus BK Virus QS-RGQ kit (Non-sterile)
TW: “凱杰”阿斯特自動化BK病毒量核酸檢驗試劑組(未滅菌)
Risk Class 1
MD

Registration Details

3bb7208441c760bd1ff4828c4c73a33d

Ministry of Health Medical Device Import No. 020206

DHA09402020605

Company Information

Germany

Product Details

This product must be used with QIAsymphony SP/AS and Rotor-Gene Q instruments to quantify BK virus DNA in human biological samples in vitro using polymerase chain reaction (PCR).

C Immunology and microbiology devices

C9999 Other

Imported from abroad

Dates and Status

Mar 19, 2019

Mar 19, 2024