"Gretel" Pylori reagent (unsterilized) - Taiwan Registration 9974fb7fd804d7fc6a28d929ba95c4ba
Access comprehensive regulatory information for "Gretel" Pylori 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 9974fb7fd804d7fc6a28d929ba95c4ba and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is GREAT BIOTECH 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 devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
C Immunology and microbiology
C.0003 ่บๆๆกฟ่ๅฑฌ่กๆธ ่ฉฆๅ
Domestic;; Contract manufacturing
Dates and Status
Aug 31, 2017
Aug 31, 2027