Taiwan FDA registration 7815f53031c7ba76c4a94b3791cb6e93
Berger Helicobacter pylori IgG enzyme immunoassay group (unsterilized)
TW: 伯杰幽門螺旋桿菌IgG酵素免疫分析組(未滅菌)
Registration details
- Analysis ID
- 7815f53031c7ba76c4a94b3791cb6e93
- Customs Code
- DHA04400590907
Company information
- Manufacturer
- BIOCHECK, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
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
- import
Dates and status
- Registration Date
- May 25, 2007
- Expiry Date
- May 25, 2027
About this record
Access comprehensive regulatory information for Berger Helicobacter pylori IgG enzyme immunoassay group (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7815f53031c7ba76c4a94b3791cb6e93 and manufactured by BIOCHECK, INC.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices