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“Immucor” PanoscreenⅠ,Ⅱ and Ⅲ - Taiwan Registration 4df802a2a455c2c4e5831ac51e11c154

Access comprehensive regulatory information for “Immucor” PanoscreenⅠ,Ⅱ and Ⅲ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4df802a2a455c2c4e5831ac51e11c154 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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4df802a2a455c2c4e5831ac51e11c154
Registration Details
Taiwan FDA Registration: 4df802a2a455c2c4e5831ac51e11c154
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Device Details

“Immucor” PanoscreenⅠ,Ⅱ and Ⅲ
TW: “依免可” 紅血球抗體篩選試劑
Risk Class 2
MD

Registration Details

4df802a2a455c2c4e5831ac51e11c154

Ministry of Health Medical Device Import No. 027709

DHA05602770907

Company Information

United States

Product Details

Detection of unanticipated red blood cell antibodies.

B Hematology and pathology devices

B9650 Quality control equipment for blood bank reactors

Imported from abroad

Dates and Status

Oct 07, 2015

Oct 07, 2025