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“Immucor” corQC Test System - Taiwan Registration 3fe502bab76c8c0af4e056ef79258564

Access comprehensive regulatory information for “Immucor” corQC Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fe502bab76c8c0af4e056ef79258564 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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3fe502bab76c8c0af4e056ef79258564
Registration Details
Taiwan FDA Registration: 3fe502bab76c8c0af4e056ef79258564
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Device Details

“Immucor” corQC Test System
TW: “依免可”核心品管試驗系統
Risk Class 2
MD

Registration Details

3fe502bab76c8c0af4e056ef79258564

Ministry of Health Medical Device Import No. 030072

DHA05603007209

Company Information

United States

Product Details

Used for routine quality control evaluation of blood bank reagents.

B Hematology and pathology devices

B9650 Quality control equipment for blood bank reactors

Imported from abroad

Dates and Status

Oct 13, 2017

Oct 13, 2027