Taiwan FDA registration e8d0f36172aa328b14d629c2c353fe62
Sanmeng creatinine liquid test system
TW: 三盟 肌酸酐液體試驗系統
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER·Registered Dec 17, 2009 – Dec 17, 2014CancelledRegistration details
- Analysis ID
- e8d0f36172aa328b14d629c2c353fe62
- Customs Code
- DHA00602074802
Company information
- Manufacturer
- FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER
- Manufacturer Country
- United States
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- 用來在自動臨床化學分析儀上體外定量測定人體血清中的肌酸酐(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
- Dec 17, 2009
- Expiry Date
- Dec 17, 2014
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Sanmeng creatinine liquid test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8d0f36172aa328b14d629c2c353fe62 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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