Taiwan FDA registration 833b27840c2168f975231f9dee99d3cd

H. pylori antigen detection reagent (unsterilized)

TW: 速得百森幽門螺旋桿菌抗原檢測試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·SD BIOSENSOR, Inc.·Registered May 31, 2022 – May 31, 2027Active
Registration details
Analysis ID
833b27840c2168f975231f9dee99d3cd
Customs Code
DHA09402281705
Company information
Manufacturer
SD BIOSENSOR, Inc.
Manufacturer Country
Korea, Republic of
Authorized Representative
CREATIVE LIFE SCIENCE CO., LTD.
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
Input;; QMS/QSD
Dates and status
Registration Date
May 31, 2022
Expiry Date
May 31, 2027
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 833b27840c2168f975231f9dee99d3cd and manufactured by SD BIOSENSOR, Inc.. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FIRSTEP BIORESEARCH 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