Taiwan FDA registration d205048a71e785de34116e7e63316981
Fujifilm blood nucleic acid preparation whole blood nucleic acid extraction kit
TW: 富士血液核酸製備全血核酸萃取套件
Taiwan·Risk Class 1·FUJIFILM EUROPE GMBH·Registered Oct 08, 2010 – Oct 08, 2015CancelledRegistration details
- Analysis ID
- d205048a71e785de34116e7e63316981
- Customs Code
- DHA04400933109
Company information
- Manufacturer
- FUJIFILM EUROPE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HUNG CHONG CORP.
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
- Oct 08, 2010
- Expiry Date
- Oct 08, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Fujifilm blood nucleic acid preparation whole blood nucleic acid extraction kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d205048a71e785de34116e7e63316981 and manufactured by FUJIFILM EUROPE GMBH. The authorized representative in Taiwan is HUNG CHONG CORP..
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