"Pushen" progesterone test reagent (unsterilized) - Taiwan Registration f002c28601d54ae98e9e6f151be194af
Access comprehensive regulatory information for "Pushen" progesterone test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f002c28601d54ae98e9e6f151be194af and manufactured by GENERAL BIOLOGICALS CORP.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GENERAL BIOLOGICALS CORP., 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.
Device Details
Product Details
Limited to the first level of identification scope of the progesterone test system (A.1620) of the classification and grading management measures for medical devices.
A Clinical chemistry and clinical toxicology
A.1620 Progesterone testing system
Domestic
Dates and Status
Jun 04, 2014
Jun 04, 2024