Liquichek Urine Toxicology Control
Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Aug 22, 2016 – Aug 22, 2026Active- Analysis ID
- be80cf5d8cd4fa0e8ca3235754d516dd
- License Form
- Ministry of Health Medical Device Import No. 028477
- Customs Code
- DHA05602847704
- Manufacturer
- BIO-RAD LABORATORIES
- Manufacturer Country
- United States
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
- Intended Use
- This product is used to monitor the quality control of laboratory urine toxicity immunoassay screening test 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
- Registration Date
- Aug 22, 2016
- Expiry Date
- Aug 22, 2026
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Access comprehensive regulatory information for Liquichek 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 be80cf5d8cd4fa0e8ca3235754d516dd and manufactured by BIO-RAD LABORATORIES. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BIO-RAD LABORATORIES, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.