Taiwan FDA registration 5d14db268deab84c56d820dc092ed601
Liquichek Urine Toxicology Control S1S,S2S
TW: 立可測 尿液毒物品管液
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Jul 19, 2016 – Jul 19, 2026ExpiredRegistration details
- Analysis ID
- 5d14db268deab84c56d820dc092ed601
- License Form
- Ministry of Health Medical Device Import No. 028459
- Customs Code
- DHA05602845902
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 intended to monitor the performance of the laboratory in performing urine toxicase immunoassay screening steps.
- 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
- Jul 19, 2016
- Expiry Date
- Jul 19, 2026
About this record
Access comprehensive regulatory information for Liquichek Urine Toxicology Control S1S,S2S in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5d14db268deab84c56d820dc092ed601 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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