Taiwan FDA registration e53c4b79803eecf97cea4a842a33aa2a

H. pylori antigen detection reagent (unsterilized)

TW: 聯華幽門螺旋桿菌抗原檢測試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·FIRSTEP BIORESEARCH INC.·Registered Dec 18, 2009 – Dec 18, 2029Active
Registration details
Analysis ID
e53c4b79803eecf97cea4a842a33aa2a
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
FIRSTEP BIORESEARCH INC.
Product details
Intended Use
Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.0003 螺旋桿菌屬血清試劑
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Dec 18, 2009
Expiry Date
Dec 18, 2029
Companies making similar products

Top companies providing products similar to "H. pylori antigen detection reagent (unsterilized)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for H. pylori antigen detection 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 e53c4b79803eecf97cea4a842a33aa2a and manufactured by FIRSTEP BIORESEARCH INC.. The authorized representative in Taiwan is FIRSTEP BIORESEARCH INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SD BIOSENSOR, Inc., 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations