Taiwan FDA registration 2800ec9eb1394f7c61224a754a4adf19
"QIAGEN" artus c. difficile QS-RGQ MDx Kit (Non-sterile)
TW: "凱杰" 阿特斯困難梭狀芽孢桿菌檢驗試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·QIAGEN GMBH·Registered Aug 04, 2015 – Aug 04, 2020CancelledRegistration details
- Analysis ID
- 2800ec9eb1394f7c61224a754a4adf19
- License Form
- Ministry of Health Medical Device Import No. 015549
- Customs Code
- DHA09401554902
Company information
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- QIAGEN TAIWAN COMPANY LIMITED
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 04, 2015
- Expiry Date
- Aug 04, 2020
- Cancellation Date
- May 06, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "QIAGEN" artus c. difficile QS-RGQ MDx 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 2800ec9eb1394f7c61224a754a4adf19 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
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