Taiwan FDA registration 3bb7208441c760bd1ff4828c4c73a33d
“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)
Taiwan·Risk Class 1·MD·QIAGEN GMBH·Registered Mar 19, 2019 – Mar 19, 2024ExpiredRegistration details
- Analysis ID
- 3bb7208441c760bd1ff4828c4c73a33d
- License Form
- Ministry of Health Medical Device Import No. 020206
- Customs Code
- DHA09402020605
Company information
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
Product details
- Intended Use
- 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).
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 19, 2019
- Expiry Date
- Mar 19, 2024
About this record
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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