"Instrument Lab" quality control solution (unsterilized) - Taiwan Registration 91951a89b452733eb030498463dd09e4
Access comprehensive regulatory information for "Instrument Lab" quality control solution (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 91951a89b452733eb030498463dd09e4 and manufactured by INSTRUMENTATION LABORATORY CO.,. The authorized representative in Taiwan is Werfen Taiwan Limited.
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
Dec 21, 2006
Dec 21, 2026

