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“Immucor” Anti-Jka (Monoclonal) Gamma-clone - Taiwan Registration 5bf5c3ac481aa790565c0e1a5beacebc

Access comprehensive regulatory information for “Immucor” Anti-Jka (Monoclonal) Gamma-clone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bf5c3ac481aa790565c0e1a5beacebc 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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5bf5c3ac481aa790565c0e1a5beacebc
Registration Details
Taiwan FDA Registration: 5bf5c3ac481aa790565c0e1a5beacebc
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Device Details

“Immucor” Anti-Jka (Monoclonal) Gamma-clone
TW: “依免可” 抗Jka血型試劑(單株抗體)
Risk Class 2
MD

Registration Details

5bf5c3ac481aa790565c0e1a5beacebc

Ministry of Health Medical Device Import No. 027900

DHA05602790000

Company Information

United States

Product Details

Suitable for the detection of red blood cell Jka (Jk1) antigen in IVF tests.

B Hematology and pathology devices

B4020 Analyze specific reagents

Imported from abroad

Dates and Status

Nov 03, 2015

Nov 03, 2025