Taiwan FDA registration cde6142ada93e601196887a48162f70e
Desay creatinine liquid kit
TW: 德賽肌酐液體試劑盒
Taiwan·Risk Class 2·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Jan 04, 2006 – Jan 04, 2016CancelledRegistration details
- Analysis ID
- cde6142ada93e601196887a48162f70e
- Customs Code
- DHA00601580701
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD.
Product details
- Intended Use
- It is used for in vitro quantitative measurement of human serum, blood or urine creatinine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1225 肌氨酸酐試驗系統(Creatininetestsystem)
- Import Information
- import
Dates and status
- Registration Date
- Jan 04, 2006
- Expiry Date
- Jan 04, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Desay creatinine liquid kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cde6142ada93e601196887a48162f70e and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD..
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