Taiwan FDA registration 0440c300f9469159d565a78cb037da46
VIROTROL HIV-1 Ag
TW: 威樂準 愛滋病毒第一型抗原品管液
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Sep 01, 2017 – Sep 01, 2027ActiveRegistration details
- Analysis ID
- 0440c300f9469159d565a78cb037da46
- License Form
- Ministry of Health Medical Device Import No. 029841
- Customs Code
- DHA05602984104
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 used as a quality control solution that has not been analyzed for reactivity in the in vitro antigen assay analysis procedure of human human immunodeficiency (HIV-1).
- 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
- Sep 01, 2017
- Expiry Date
- Sep 01, 2027
About this record
Access comprehensive regulatory information for VIROTROL HIV-1 Ag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0440c300f9469159d565a78cb037da46 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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