Taiwan FDA registration a8dc7ca33776e632e20fdcaf4a1782fa
"Kuaian" micronucleic acid purification test group (unsterilized)
TW: "快安"微量核酸純化試藥組(未滅菌)
Taiwan·Risk Class 1·QIAGEN GMBH·Registered Mar 01, 2011 – Mar 01, 2016CancelledRegistration details
- Analysis ID
- a8dc7ca33776e632e20fdcaf4a1782fa
- Customs Code
- DHA04400995600
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
- Mar 01, 2011
- Expiry Date
- Mar 01, 2016
- 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 "Kuaian" micronucleic acid purification test group (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a8dc7ca33776e632e20fdcaf4a1782fa and manufactured by QIAGEN GMBH. The authorized representative in Taiwan is TAIGEN BIOSCIENCE CORPORATION.
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