Taiwan FDA registration d95258b09fda96f2f4b30ed3d9490986
VIROTROL Syphilis LR-A
TW: 威樂準 梅毒品管液
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Jun 22, 2017 – Jun 22, 2027ActiveRegistration details
- Analysis ID
- d95258b09fda96f2f4b30ed3d9490986
- License Form
- Ministry of Health Medical Device Import No. 029586
- Customs Code
- DHA05602958601
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 precision quality control solution, which can be used as an in vitro diagnostic analysis procedure for qualitative determination of Treponema pallidum 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 22, 2017
- Expiry Date
- Jun 22, 2027
About this record
Access comprehensive regulatory information for VIROTROL Syphilis LR-A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d95258b09fda96f2f4b30ed3d9490986 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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