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"Siemens" hepatitis A antibody test set - Taiwan Registration bf9b0627c9096c103611bf9b95e2a0bb

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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bf9b0627c9096c103611bf9b95e2a0bb
Registration Details
Taiwan FDA Registration: bf9b0627c9096c103611bf9b95e2a0bb
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Device Details

"Siemens" hepatitis A antibody test set
TW: โ€œ่ฅฟ้–€ๅญโ€ Aๅž‹่‚็‚ŽๆŠ—้ซ”ๆชข้ฉ—่ฉฆๅŠ‘็ต„
Risk Class 3

Registration Details

bf9b0627c9096c103611bf9b95e2a0bb

DHA00602140605

Company Information

United States

Product Details

Quantitative detection of hepatitis A virus antibodies in human serum and plasma.

B Hematology, pathology, and genetics

B.4020 Analysis of specific tests

import

Dates and Status

Aug 24, 2010

Aug 24, 2025

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