Taiwan FDA registration 838cbf00837bfa3dd9e2a37fd365dc03
VIROTROL HIV-1 gO
TW: 威樂準 愛滋病毒第1型抗體品管液
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Sep 12, 2017 – Sep 12, 2027ActiveRegistration details
- Analysis ID
- 838cbf00837bfa3dd9e2a37fd365dc03
- License Form
- Ministry of Health Medical Device Import No. 029851
- Customs Code
- DHA05602985107
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 mainly an unspecified but reactive quality control solution, which is used as an in vitro assay analysis procedure for detecting HIV type 1 antibodies in human serum or plasma.
- 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 12, 2017
- Expiry Date
- Sep 12, 2027
About this record
Access comprehensive regulatory information for VIROTROL HIV-1 gO in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 838cbf00837bfa3dd9e2a37fd365dc03 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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