Taiwan FDA registration d528d3564cbb7be1ee1ea3bcedfba84a
VIROTROL HIV-2
TW: 威樂準 愛滋病毒第二型品管液
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Jun 21, 2017 – Jun 21, 2027ActiveRegistration details
- Analysis ID
- d528d3564cbb7be1ee1ea3bcedfba84a
- License Form
- Ministry of Health Medical Device Import No. 029585
- Customs Code
- DHA05602958502
Company information
- Manufacturer
- BIO-RAD LABORATORIES
- Manufacturer Country
- United States
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- This product is an unanalyzed reactive quality control solution and can be used as an in vitro analysis procedure for the evaluation of human HIV type 2 antibodies. This product can be used as a tool to estimate precision and can be used to detect systematic deviations in specific laboratory test procedures.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 21, 2017
- Expiry Date
- Jun 21, 2027
About this record
Access comprehensive regulatory information for VIROTROL HIV-2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d528d3564cbb7be1ee1ea3bcedfba84a and manufactured by BIO-RAD LABORATORIES. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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