Taiwan FDA registration 43bcffaa883fbf335c8956bfa952f7bf
Liquichek Qualitative Urine Toxicology Control
TW: 立可測 定性尿液毒物品管液
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Aug 26, 2016 – Aug 26, 2026ActiveRegistration details
- Analysis ID
- 43bcffaa883fbf335c8956bfa952f7bf
- License Form
- Ministry of Health Medical Device Import No. 028481
- Customs Code
- DHA05602848108
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 a known quality control substance intended to monitor laboratories for performing qualitative urine toxicity 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
- Aug 26, 2016
- Expiry Date
- Aug 26, 2026
About this record
Access comprehensive regulatory information for Liquichek Qualitative Urine Toxicology Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43bcffaa883fbf335c8956bfa952f7bf 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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