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“Immucor” Anti-K (Human Monoclonal) Series 2 - Taiwan Registration dec680a9cfcf76ca4c9ff9cadd33a8fe

Access comprehensive regulatory information for “Immucor” Anti-K (Human Monoclonal) Series 2 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dec680a9cfcf76ca4c9ff9cadd33a8fe 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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Registration Details
Taiwan FDA Registration: dec680a9cfcf76ca4c9ff9cadd33a8fe
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Device Details

“Immucor” Anti-K (Human Monoclonal) Series 2
TW: “依免可” 抗K血清(系列2)
Risk Class 2
MD

Registration Details

dec680a9cfcf76ca4c9ff9cadd33a8fe

Ministry of Health Medical Device Import No. 025857

DHA05602585702

Company Information

United States

Product Details

This product is suitable for the detection of K antigen (kell or KEL1) by slide, test tube and microdisc method.

B Hematology and pathology devices

B9175 Automated Blood Sorting and Antibody Testing System

Imported from abroad

Dates and Status

Jan 16, 2014

Jan 16, 2029