Taiwan FDA registration a16f32e425f6eb91c670ad6a2cf07506

Xiec Herpes simplex virus type 1 immunoglobulin M antibody reagent

TW: 協克單純疱疹病毒1型免疫球蛋白M抗體試劑

Taiwan·Risk Class 2·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Apr 19, 2010 – Apr 19, 2025Expired

Registration details

Analysis ID: a16f32e425f6eb91c670ad6a2cf07506
Customs Code: DHA00602097704

Company information

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

Product details

Intended Use: This reagent is used to semi-quantitatively detect human serum or plasma HSV-1-specific glycoprotein gC1 IgM antibodies using ELISA analysis method.
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: Apr 19, 2010
Expiry Date: Apr 19, 2025

About this record

Access comprehensive regulatory information for Xiec Herpes simplex virus type 1 immunoglobulin M 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 a16f32e425f6eb91c670ad6a2cf07506 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.