Taiwan FDA registration bf9b0627c9096c103611bf9b95e2a0bb

"Siemens" hepatitis A antibody test set

TW: “西門子” A型肝炎抗體檢驗試劑組
Taiwan flagTaiwan·Risk Class 3·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Aug 24, 2010 – Aug 24, 2025Expired
Registration details
Analysis ID
bf9b0627c9096c103611bf9b95e2a0bb
Customs Code
DHA00602140605
Company information
Manufacturer Country
United States
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
Quantitative detection of hepatitis A virus antibodies in human serum and plasma.
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.4020 Analysis of specific tests
Import Information
import
Dates and status
Registration Date
Aug 24, 2010
Expiry Date
Aug 24, 2025
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About this record

Access comprehensive regulatory information for "Siemens" hepatitis A antibody test set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bf9b0627c9096c103611bf9b95e2a0bb and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS HEALTHCARE DIAGNOSTICS 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.

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