Taiwan FDA registration dab724ab20e8d39fc26fa810f074e5c7
Sanmeng urea liquid test system
TW: 三盟 尿素液體試驗系統
Taiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER·Registered Dec 18, 2009 – Dec 18, 2014CancelledRegistration details
- Analysis ID
- dab724ab20e8d39fc26fa810f074e5c7
- Customs Code
- DHA00602075002
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
- It is used to quantify urea in human serum, blood or urine in vitro
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1770 尿素氮試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 18, 2009
- Expiry Date
- Dec 18, 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 urea 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 dab724ab20e8d39fc26fa810f074e5c7 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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