Taiwan FDA registration e7942058763e884d7400997ede72c349

Xiec Herpes simplex virus 1+2 IgG antibody reagent

TW: 協克單純疱疹病毒1+2型IgG抗體試劑

Taiwan·Risk Class 2·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Jan 08, 2010 – Jan 08, 2025Expired

Registration details

Analysis ID: e7942058763e884d7400997ede72c349
Customs Code: DHA00602078903

Company information

Manufacturer: EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
Manufacturer Country: Germany
Authorized Representative: SEEKERS BIOMEDICAL CO., LTD.

Product details

Intended Use: Semi-quantitative or quantitative in vitro assays to determine the antibody titer of herpes simplex virus 1+2 IgG in serum.
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: Jan 08, 2010
Expiry Date: Jan 08, 2025

About this record

Access comprehensive regulatory information for Xiec Herpes simplex virus 1+2 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 e7942058763e884d7400997ede72c349 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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