Taiwan FDA registration b8f7f99505d0bad73033e6f8a01e6173
Xiec herpes simplex virus type I IgG antibody reagent
TW: 協克單純疱疹病毒I型IgG抗體試劑
Taiwan·Risk Class 2·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Dec 31, 2009 – Dec 31, 2024ExpiredRegistration details
- Analysis ID
- b8f7f99505d0bad73033e6f8a01e6173
- Customs Code
- DHA00602076900
Company information
- Manufacturer
- EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
- Manufacturer Country
- Germany
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- This product provides a half-quantitative or quantitative in vitro assay for the determination of antibody titer of herpes simplex virus type 1 IgG in serum or plasma.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3305 Seroanalysis of monoperiasis virus
- Import Information
- import
Dates and status
- Registration Date
- Dec 31, 2009
- Expiry Date
- Dec 31, 2024
About this record
Access comprehensive regulatory information for Xiec herpes simplex virus type I IgG antibody reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b8f7f99505d0bad73033e6f8a01e6173 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
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