Taiwan FDA registration 65f75fd909a881e6b853f71077c28399
Helen Na Interface Fluid
TW: 海倫那界面液
Taiwan·Risk Class 1·HELENA LABORATORIES, INC.·Registered Oct 20, 2005 – Oct 20, 2015CancelledRegistration details
- Analysis ID
- 65f75fd909a881e6b853f71077c28399
- Customs Code
- DHA04400110703
Company information
- Manufacturer
- HELENA LABORATORIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- The interfacial conductive fluid for the electrophoresis tank.
- 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 20, 2005
- Expiry Date
- Oct 20, 2015
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Helen Na Interface Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 65f75fd909a881e6b853f71077c28399 and manufactured by HELENA LABORATORIES, INC.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
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