Taiwan FDA registration 4907e3123ded9ab2bed80c79e0594399
Kuai'an County ultra-blood nucleic acid purification test group
TW: 快安郡超血液核酸純化試藥組
Taiwan·Risk Class 1·QIAGEN GMBH·Registered Nov 04, 2010 – Nov 04, 2015CancelledRegistration details
- Analysis ID
- 4907e3123ded9ab2bed80c79e0594399
- Customs Code
- DHA04400945807
Company information
- Manufacturer
- QIAGEN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIGEN BIOSCIENCE CORPORATION
Product details
- Intended Use
- Limited to the first level identification scope of "General Purpose Reaction Reagents (B.4010)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.4010 Reaction Reagents for General Purposes
- Import Information
- import
Dates and status
- Registration Date
- Nov 04, 2010
- Expiry Date
- Nov 04, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Kuai'an County ultra-blood nucleic acid purification test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4907e3123ded9ab2bed80c79e0594399 and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is TAIGEN BIOSCIENCE CORPORATION.
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