Taiwan FDA registration fcdd1f0b06b1f832a8375e1ef0f993e1
“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)
Taiwan·Risk Class 1·MD·QIAGEN GMBH·Registered Jun 05, 2020 – Jun 05, 2025ExpiredRegistration details
- Analysis ID
- fcdd1f0b06b1f832a8375e1ef0f993e1
- License Form
- Ministry of Health Medical Device Import No. 021622
- Customs Code
- DHA09402162201
Company information
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification range of "Epstein-Barr virus serum reagent (C.3235)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3235 Epstein-Barr virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 05, 2020
- Expiry Date
- Jun 05, 2025
About this record
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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