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“QIAGEN” artus CMV RG PCR Kit - Taiwan Registration f61c675e8962d7dce04fba28daf6dec0

Access comprehensive regulatory information for “QIAGEN” artus CMV RG PCR Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f61c675e8962d7dce04fba28daf6dec0 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

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f61c675e8962d7dce04fba28daf6dec0
Registration Details
Taiwan FDA Registration: f61c675e8962d7dce04fba28daf6dec0
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Device Details

“QIAGEN” artus CMV RG PCR Kit
TW: “凱杰” 阿特斯巨細胞病毒核酸檢驗試劑套組
Risk Class 2
MD

Registration Details

f61c675e8962d7dce04fba28daf6dec0

Ministry of Health Medical Device Import No. 027347

DHA05602734702

Company Information

Germany

Product Details

This product is an in vitro nucleic acid amplification assay for the quantitative detection of CMV DNA in human plasma. This product uses polymerase chain reaction (PCR) technology and is used with a Rotor-Gene Q instrument.

C Immunology and microbiology devices

C3175 CMV serum reagent

Imported from abroad

Dates and Status

Jun 05, 2015

Jun 05, 2025