Taiwan FDA registration 7b55c43539fd3fdd80aa8780055082f6
"Qiagen" Artus EBV PCR 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 18, 2014 – Jun 18, 2019CancelledRegistration details
- Analysis ID
- 7b55c43539fd3fdd80aa8780055082f6
- License Form
- Ministry of Health Medical Device Import No. 014262
- Customs Code
- DHA09401426203
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)
- C3235 Epstein-Barr virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 18, 2014
- Expiry Date
- Jun 18, 2019
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Qiagen" Artus EBV PCR 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 7b55c43539fd3fdd80aa8780055082f6 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.
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