Taiwan FDA registration 50a2455fed9324b7727585529606dd3c
“Bio-Rad”qUAntify Advance Control
TW: “伯瑞”肯定量進階品管液
Registration details
- Analysis ID
- 50a2455fed9324b7727585529606dd3c
- License Form
- Ministry of Health Medical Device Import No. 032482
- Customs Code
- DHA05603248202
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 for tabular analytes to monitor the precision of laboratory urine testing 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 19, 2019
- Expiry Date
- Aug 19, 2024
About this record
Access comprehensive regulatory information for “Bio-Rad”qUAntify Advance Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50a2455fed9324b7727585529606dd3c 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. 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.
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