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"Eprocexor" anti-D serum (series 5) - Taiwan Registration 62ab252db8f1242371f58c66a76f8dff

Access comprehensive regulatory information for "Eprocexor" anti-D serum (series 5) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62ab252db8f1242371f58c66a76f8dff and manufactured by IMMUCOR, INC.. The authorized representative in Taiwan is Y.H. BIOTEK 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.

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62ab252db8f1242371f58c66a76f8dff
Registration Details
Taiwan FDA Registration: 62ab252db8f1242371f58c66a76f8dff
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Device Details

"Eprocexor" anti-D serum (series 5)
TW: โ€œไพๅ…ๅฏโ€ๆŠ—D่ก€ๆธ…(็ณปๅˆ—5)
Risk Class 2

Registration Details

62ab252db8f1242371f58c66a76f8dff

DHA00602383601

Company Information

United States

Product Details

Measurement type D blood type.

B Hematology, pathology, and genetics

B.9175 Automated Blood Classification and Antibody Testing System

import

Dates and Status

Aug 07, 2012

Aug 07, 2027