"Bury" Ethanol/Ammonia External Quality Assurance Program (Unsterilized) - Taiwan Registration 9716bdfdfb46ee959b9320450800d312
Access comprehensive regulatory information for "Bury" Ethanol/Ammonia External Quality Assurance Program (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9716bdfdfb46ee959b9320450800d312 and manufactured by BIO-RAD LABORATORIES INC.. 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.
Device Details
Product Details
Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
A Clinical chemistry and clinical toxicology
A.1660 Quality control materials (analytical and non-analytical)
import
Dates and Status
Jan 17, 2013
Jan 17, 2028